2019 No. 556

Exiting The European Union

Pesticides

The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019

Made20th March 2019

Coming into force in accordance with regulation 1(1)

The Secretary of State makes these Regulations in exercise of the powers conferred by section 8(1) of, and paragraph 21 of Schedule 7 to, the European Union (Withdrawal) Act 2018 M1.

In accordance with paragraph 1(1) of Schedule 7 to the European Union (Withdrawal) Act 2018, a draft of this instrument has been laid before Parliament and approved by a resolution of each House of Parliament.

Annotations:

Marginal Citations

2018 c. 16.

PART 1Introductory

F15Citation, commencement, extent and interpretationI2391

1

These Regulations may be cited as the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019, and come into force on exit day.

F31A

Regulation 28 and Schedule 1 extend to Great Britain.

2

In these Regulations—

“Regulation (EC) No 1107/2009” means Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market;
“competent authority” and “constituent territory” have the meanings given in Article 3A of Regulation (EC) No 1107/2009 (as inserted by regulation 3(5)).

PART 2Amendment of retained direct EU legislation

CHAPTER 1Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market

Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the marketI6112

Regulation (EC) No 1107/2009 is amended in accordance with regulations 3 to 14.

in point (a), for “that Member State” substitute “ F6Great Britain ”;

i

omit paragraph 30;

j

after paragraph 31 insert—

F3031A
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
31B
‘approvals register’ means the register maintained in accordance with Article 27A;
31C
‘unacceptable co-formulants register’ means the register maintained in accordance with Article 27B;
31D
‘EU-derived domestic legislation’ has the meaning given by section 2(2) of the European Union (Withdrawal) Act 2018;

5

After Article 3 insert—

Article 3ADefinitions: competent authority, constituent territory and appropriate authority
1
In this Regulation, a reference to a competent authority or a constituent territory is to be interpreted in accordance with the provisions of this Article.
2
The Secretary of State is the competent authority for the constituent territory of England.
3
The Welsh Ministers are the competent authority for the constituent territory of Wales.
4
The Scottish Ministers are the competent authority for the constituent territory of Scotland.
F765
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6
In this Regulation, “the appropriate authority” means—
a
for regulations applying in relation to England, the Secretary of State;
b
for regulations applying in relation to Wales, the Welsh Ministers;
c
for regulations applying in relation to Scotland, the Scottish Ministers;
F76d
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
7
But the appropriate authority is the Secretary of State if consent is given by—
a
for regulations applying in relation to Wales, the Welsh Ministers;
b
for regulations applying in relation to Scotland, the Scottish Ministers;
F76c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Chapter 2I4324

1

Chapter 2 is amended as follows.

2

In Article 4—

a

in paragraphs 2(a) and 3(b) and (e), for “by the Authority” substitute “ in accordance with paragraph 8 ”;

b

in paragraph 4, for “Article 29(6)” substitute “ Article 29(6)(a) which apply to each constituent territory to which approval of the active substance relates ”;

c

in paragraph 7—

i

in the third subparagraph—

aa

for “Member States” substitute “ A competent authority ”;

bb

for “their” substitute “ its constituent ”;

ii

in the fourth subparagraph—

aa

for “they” substitute “ the competent authority ”;

bb

for “transmit that plan to the Commission” substitute “ publish that plan in a manner which the competent authority considers appropriate ”;

d

after paragraph 7 insert—

8
For the purposes of paragraphs 2(a) and 3(b) and (e), scientific methods are accepted if they are accepted—
a
in relation to England, by the Secretary of State;
b
in relation to Wales—
i
by the Secretary of State with the consent of the Welsh Ministers, or
ii
by the Welsh Ministers;
c
in relation to Scotland—
i
by the Secretary of State with the consent of the Scottish Ministers, or
ii
by the Scottish Ministers;
F65d
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3

For Article 5 substitute—

Article 5First approval
1
First approval must be for a period not exceeding—
a
10 years for an active substance, safener or synergist;
b
15 years for a low-risk active substance (see Article 22);
c
7 years for a candidate for substitution (see Article 24).
2
Paragraph 1 is subject to Article 17.
3
Approval for a basic substance (see Article 23) is for an unlimited period.

4

In Article 6—

a

the existing text becomes paragraph 1;

b

in that paragraph, in point (f), for the words from “Member States” to “(the Authority)” substitute “ each specified competent authority within a specified period ”;

c

after that paragraph insert—

2
A competent authority may request from a specified competent authority a copy of any confirmatory information received in accordance with paragraph 1(f), which the specified competent authority must provide as soon as reasonably practicable.
3
In this Article, “specified” means specified in the condition referred to in paragraph 1(f).

5

In Article 7—

a

for paragraph 1 substitute—

1
An application for the approval of an active substance may be submitted by the producer of the active substance to a competent authority.
1A
An application for an amendment to the conditions of an approval may be submitted by the producer of the active substance to a competent authority for a constituent territory to which the approval applies.
1B
A joint application may be submitted under paragraph 1 or 1A by an association of producers designated by the producers for the purpose of compliance with this Regulation.
1C
For the purposes of this Subsection, “the assessing competent authority” in relation to an application is the competent authority referred to in paragraph 1 or 1A respectively, except where a transfer has been agreed under Article 12A(1).
1D
An application under paragraph 1 or 1A must be submitted together with a summary and a complete dossier as provided for in Article 8(1) and (2) or a scientifically reasoned justification for not providing certain parts of those dossiers, demonstrating that the active substance fulfils the approval criteria provided for in Article 4.

b

omit paragraph 2;

c

in paragraph 3, in the second subparagraph—

i

in the first sentence for “Member States” substitute “ The assessing competent authority ”;

ii

in the second sentence, for “rapporteur Member State” substitute “ assessing competent authority ”;

d

for paragraph 5, substitute—

5
When assessing the application the assessing competent authority may obtain independent scientific advice, where the assessing competent authority considers it appropriate to do so.

6

In Article 8—

a

in paragraph 1—

i

in point (a)—

aa

for “widely grown crop in each zone” substitute “ crop grown in the United Kingdom ”;

bb

omit “cover all zones or”;

cc

omit “which is not widely grown”;

ii

in point (b), after “substance” insert “ which apply in each of the constituent territories to which the application relates ”;

iii

in point (c), after “product” insert “ which apply in each of the constituent territories to which the application relates ”;

b

omit paragraph 3;

c

for paragraph 4 substitute—

4
The appropriate authority may by regulations prescribe the data requirements for—
a
one or more active substances, safeners and synergists for the purposes of paragraph 1(b);
b
plant protection products for the purposes of paragraph 1(c).

a

for the first subparagraph substitute—

a
The assessing competent authority must circulate the draft assessment report to the applicant and the other competent authorities at the latest 30 days after its completion. The assessing competent authority may ask the applicant to circulate any updated dossier to the assessing competent authority and the other competent authorities.

b

the existing second and third subparagraphs become points (b) and (c);

c

in those points (b) and (c), for “Authority” substitute “ assessing competent authority ”.

13

In paragraph 2—

a

omit the first subparagraph;

b

in the second subparagraph—

i

in the first sentence—

aa

for “Authority” substitute “ assessing competent authority ”;

bb

for “, the Member States and the Commission” substitute “ and the other competent authorities, ”;

ii

for the second sentence substitute—

In the event that independent scientific advice is obtained by the assessing competent authority in accordance with Article 7(5), the 120-day period must be extended by 90 days.

c

in the third subparagraph, for “Authority” substitute “ assessing competent authority ”.

14

In paragraph 3—

a

the existing first subparagraph becomes point (a);

b

in that point (a)—

i

for “Authority” in the first place it occurs substitute “ assessing competent authority ”;

ii

for “Member States, the Commission and the Authority” substitute “ assessing competent authority and the other competent authorities ”;

c

for the second subparagraph, substitute—

b
The assessing competent authority must assess the additional information, and for that purpose the period provided for in paragraph 2 may be extended by a maximum of 60 days.

d

the existing third subparagraph becomes point (c);

e

in that point (c)—

i

for “Authority” substitute “ assessing competent authority ”;

ii

omit “ask the Commission to”;

iii

omit “Community” in both places it occurs.

15

In paragraph 4, for “Authority” substitute “ assessing competent authority ”.

16

Omit paragraph 5.

17

In paragraph 6, for the words from “limits for the Authority's” to “Article 11 and” substitute “limit”.

18

Omit paragraphs 7 and 8.

19

After Article 12 insert—

Article 12AApplication for approval: transfer of assessment functions
1
The assessing competent authority may by agreement transfer the functions listed in paragraph 2 in relation to an application for approval to another competent authority for a constituent territory in relation to which the same application has been made, and upon transfer that competent authority is the assessing competent authority for the purposes of this Subsection.
2
For the purposes of paragraph 1 the functions are the functions of the assessing competent authority under Articles 7(3) and (5), 9, 10, 11 and 12.
3
Following a transfer under paragraph 1, the assessing competent authority must notify the applicant of the transfer.
4
A transfer in accordance with paragraph 1 does not—
a
affect anything done by the assessing competent authority prior to transfer;
b
affect the timing of any requirements placed on the assessing competent authority under this Subsection.

20

For Article 13, substitute—

Article 13Approval Decision
1
Within six months of the relevant conclusion date, a competent authority for a constituent territory to which the application relates must decide to do one of the following—
a
approve the active substance, subject to conditions or restrictions, as referred to in Article 6(1), where appropriate;
b
amend the conditions of the approval; or
c
refuse to approve the active substance.
2
In making a decision under paragraph 1, the competent authority must have regard to—
a
the conclusion of the assessing competent authority;
b
any comments received by the assessing competent authority in relation to the application, including any environmental monitoring information submitted by an appropriate agency;
c
where the competent authority considers it appropriate to obtain it, any independent scientific advice obtained;
d
where the conditions laid down in Article 7(1) of Regulation (EC) No 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety are relevant, the precautionary principle;
e
any other matters which the competent authority considers relevant to the competent authority's decision.
3
As soon as reasonably practicable after making a decision under paragraph 1, the competent authority must—
a
notify the applicant and the other competent authorities in writing of the decision and the reasons for it, and
b
update the approvals register accordingly.
4
The Secretary of State may make a decision under paragraph 1 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F102c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5
Where the Secretary of State makes a decision in accordance with paragraph 4—
a
a reference in paragraphs 2 and 3 to the competent authority is to be read as a reference to the Secretary of State;
b
paragraph 3(a) is to be read as if “other” were omitted.
6
In paragraph 1, the “relevant conclusion date” means—
a
where the competent authority is the assessing competent authority, the date on which the competent authority adopts a conclusion under Article 12(2);
b
otherwise, the date on which the competent authority receives the conclusion of the assessing competent authority in accordance with Article 12(2).
7
In paragraph 2(b), “appropriate agency” means one of the following—
a
the Environment Agency;
b
the Natural Resources Body for Wales;
c
the Scottish Environment Protection Agency;
F102d
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

21

In Article 14—

a

in paragraph 1, in the third subparagraph, for “Article 6” substitute “ Article 6(1) ”;

b

for paragraph 2 substitute—

2
The renewal of the approval must be for a period not exceeding—
a
where the active substance is covered by Article 4(7), 5 years;
b
for a candidate for substitution (see Article 24), 7 years;
c
otherwise, 15 years.
3
Paragraph 2 is subject to Article 17.

22

In Article 15—

a

in paragraph 1, for the words from “Member State” to “and the Authority” substitute “ competent authority for a constituent territory in relation to which the active substance is approved ”;

b

after paragraph 1 insert—

1A
For the purposes of this Subsection, “the assessing competent authority” in relation to an application is the competent authority referred to in paragraph 1, except where a transfer has been agreed under Article 15A(1).

c

after paragraph 2 insert—

3
The assessing competent authority must notify the other competent authorities as soon as reasonably practicable after receipt of an application under paragraph 1.
4
A competent authority which receives a notification under paragraph 3 may request in writing from the applicant a copy of the application and any accompanying information, which the applicant must provide as soon as reasonably practicable.

23

After Article 15 insert—

Article 15AApplications for renewal: transfer of assessment
1
The assessing competent authority may by agreement transfer the function of assessing an application for renewal to another competent authority for a constituent territory in relation to which the active substance to be renewed is approved, and upon transfer that competent authority is the assessing competent authority for that application for the purposes of the renewal provisions.
2
The application for renewal and any supporting dossiers or information must be transferred at the same time as the transfer under paragraph 1.
3
Following a transfer under paragraph 1, the assessing competent authority must notify the applicant of the transfer.
4
A transfer in accordance with paragraph 1 does not—
a
affect anything done by the assessing competent authority prior to transfer;
b
affect the timing of any requirements placed on the assessing competent authority under the renewal provisions.
5
In this Article, the “renewal provisions” means the provisions of—
a
this Subsection, and
b
Commission Implementing Regulation (EU) No 844/2012 setting out the provisions necessary for the implementation of the renewal procedure for active substances.

24

In Article 16, for “Authority” substitute “ assessing competent authority ”.

25

In Article 17—

a

for the first paragraph, substitute—

1
Where for reasons beyond the control of the applicant it appears to a competent authority that the approval is likely to expire before a decision has been taken on renewal, the competent authority must extend the approval period by a further period sufficient to examine the application.

b

omit the second paragraph;

c

the existing third paragraph becomes paragraph 3;

d

after that paragraph 3, insert—

4
As soon as reasonably practicable after extending the approval period in accordance with the first paragraph, the competent authority must—
a
notify the applicant and the other competent authorities of the extension, and
b
update the approvals register accordingly.
5
The Secretary of State may extend approval under paragraph 1 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F77c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6
Where the Secretary of State extends approval in accordance with paragraph 5, paragraph 4 is to be read as if—
a
in the words before point (a), the reference to the competent authority were a reference to the Secretary of State;
b
in point (a), “other” were omitted.

26

In Article 18—

a

the existing first paragraph becomes paragraph 1;

b

in that paragraph 1—

i

in the first sentence, for “The Commission” substitute “ A competent authority ”;

ii

in the second sentence, for “Member States, the Commission and the Authority” substitute “ competent authority ”;

c

the existing second paragraph becomes paragraph 2;

d

in that paragraph 2, omit point (f);

e

after that paragraph 2, insert—

3
The competent authority may vary or withdraw a work programme established by it.
4
The competent authority must publish the work programme and notice of any variation or withdrawal of a work programme in such manner as the competent authority thinks appropriate.
5
The Secretary of State may establish, vary or withdraw a work programme under paragraph 1 or 3 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F80c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6
Where the Secretary of State establishes, varies or withdraws a work programme in accordance with paragraph 5, a reference in paragraph 4 to the competent authority is to be read as a reference to the Secretary of State.
7
Where the Secretary of State establishes, varies or withdraws a work programme in accordance with paragraph 5 in respect of one or more competent authorities, the programme must also include an allocation of evaluation of active substances to the Secretary of State and those competent authorities, taking into account a balance in the responsibilities and work to be done among the Secretary of State and those competent authorities.
8
A competent authority may request in writing from the competent authority which receives data relating to an active substance in accordance with a work programme under this Article a copy of that data, which the competent authority must provide as soon as reasonably practicable.

27

For Articles 19 to 21 substitute—

Article 19Implementing measures
The appropriate authority may, by regulations, make provision necessary for the implementation of the renewal procedure.
Article 20Renewal decision
1
Within six months of the relevant conclusion date, a competent authority for a constituent territory to which the application relates must decide to either—
a
renew the approval of the active substance, subject to conditions or restrictions, as referred to in Article 6(1), where appropriate; or
b
refuse to renew approval of the active substance.
2
In making a decision under paragraph 1, the competent authority must have regard to—
F42a
the conclusion of the assessing competent authority and the opinion of the Agency, if any, referred to in Article 37(4) of Regulation (EC) No 1272/2008;
b
any comments received by the assessing competent authority in relation to the application, including any environmental monitoring information submitted by an appropriate agency;
c
where the competent authority considers it appropriate to obtain it, any independent scientific advice obtained;
d
where the conditions laid down in Article 7(1) of Regulation (EC) No 178/2002 of the European Parliament and of the Council are relevant, the precautionary principle;
e
any other matters which the competent authority considers relevant to the competent authority's decision.
3
Where the reasons for not renewing the approval of an active substance—
a
relate to immediate concerns for the protection of human or animal health or the environment, plant protection products containing that active substance must be withdrawn from the market immediately;
b
do not fall within point (a), the competent authority must set a grace period in respect of existing stocks of the plant protection products containing that active substance.
4
The grace period—
a
for the sale and distribution of the plant protection products must take into account the normal period of use of those plant protection products but must not exceed six months;
b
for the disposal, storage, and use of the plant protection products must be consecutive to the period described in point (a) and must not exceed one year.
5
As soon as reasonably practicable after making a decision under paragraph 1, the competent authority must—
a
notify the applicant and the other competent authorities in writing of the decision under paragraph 1, the reasons for that decision and the details of any grace period set in accordance with paragraphs 3 and 4, and
b
update the approvals register accordingly.
6
The Secretary of State may make a decision under paragraph 1 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F58c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
7
Where the Secretary of State makes a decision in accordance with paragraph 6, a reference in paragraphs 2, 3 and 5 to the competent authority is to be read as a reference to the Secretary of State.
8
In paragraph 1, the “relevant conclusion date” means—
a
where the competent authority is the assessing competent authority, the date on which the competent authority adopts a conclusion under Article 13(1) of Commission Implementing Regulation (EU) No 844/2012;
b
otherwise, the date on which the competent authority receives the conclusion of the assessing competent authority in accordance with Article 13(1) of Commission Implementing Regulation (EU) No 844/2012.
9
In paragraph 2(b), “appropriate agency” has the meaning given by Article 13(7).
Article 20AReview of further information submitted
1
Where an approval is subject to a condition in accordance with Article 6(1)(f), any confirmatory information received within the period specified in the condition must be assessed by the reviewing authority.
2
Within 6 months of receipt of the confirmatory information, the reviewing authority must—
a
assess that information, and
b
submit its assessment to the other competent authorities.
3
For the purposes of this Article, the “reviewing authority” is—
a
the competent authority specified in the condition to which the approval is subject, or
b
a competent authority to which the function of reviewing the confirmatory information is transferred in accordance with paragraph 4.
4
The reviewing authority may by agreement transfer the function of reviewing confirmatory information received to another competent authority.
5
Any confirmatory information received must be transferred at the same time as the transfer under paragraph 4.
6
Following a transfer under paragraph 4, the competent authority to which the function is transferred must notify the applicant of the transfer.
7
A transfer in accordance with paragraph 4 does not—
a
affect anything done by the reviewing authority prior to transfer;
b
affect the timing of the requirement in paragraph 2.
Article 21Review of approval
1
A competent authority may review the approval of an active substance in relation to its constituent territory at any time.
2
The competent authority must review the approval of an active substance in relation to its constituent territory where—
a
the competent authority has assessed confirmatory information as reviewing authority in accordance with Article 20A(1),
b
the competent authority receives the assessment of the reviewing competent authority in accordance with Article 20A(2)(b), or
c
further information required in accordance with a condition under Article 6(1)(f) has not been provided within the period specified in the condition.
3
Where the competent authority considers that—
a
in light of new scientific and technical knowledge or the assessment of the reviewing authority in accordance with Article 20A, there are indications that the active substance no longer satisfies the approval criteria provided for in Article 4, or
b
further information required in accordance with a condition under Article 6(1)(f) has not been provided
the competent authority must inform each of the other competent authorities and the producer of the active substance accordingly, setting a period for the submission of comments.
4
The competent authority may obtain independent scientific advice, where the competent authority considers it appropriate to do so.
5
Where the competent authority concludes, having considered comments received during the period set in accordance with paragraph 3 and any other information or matters that the competent authority considers relevant to the review, that paragraph 3(a) or (b) apply, the competent authority must decide to either—
a
amend the conditions or restrictions of the approval, or
b
withdraw the approval.
6
Where the reasons for withdrawing the approval of an active substance—
a
relate to immediate concerns for the protection of human or animal health or the environment, plant protection products containing that active substance must be withdrawn from the market immediately;
b
do not fall within point (a), the competent authority must set a grace period in respect of existing stocks of the plant protection products containing that active substance.
7
The grace period—
a
for the sale and distribution of the plant protection products must take into account the normal period of use of those plant protection products but must not exceed six months;
b
for the disposal, storage, and use of the plant protection products must be consecutive to the period described in point (a) and must not exceed one year.
8
As soon as reasonably practicable after making a decision under paragraph 5, the competent authority must—
a
notify the producer of the active substance and the other competent authorities in writing of the decision, the reasons for that decision, and the details of any grace period set in accordance with paragraphs 6 and 7, and
b
update the approvals register accordingly.
9
The Secretary of State may review an active substance under paragraph 1 or 2 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F58c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
10
Where the Secretary of State reviews an active substance in accordance with paragraph 9, a reference in paragraphs 3 to 6 and 8 to the competent authority is to be read as a reference to the Secretary of State.

28

For Article 22 substitute—

Article 22Low-risk active substances
1
An active substance complying with the criteria provided for in Article 4 must be approved as a low-risk active substance where—
a
that substance complies with the criteria in point 5 of Annex 2, and
b
it may be expected that plant protection products containing that substance will pose only a low risk to human and animal health and the environment as provided for in Article 47(1).
2
Articles 4 to 21 apply.
3
The appropriate authority may, by regulations, amend point 5 of Annex 2 to specify new criteria for approving an active substance as a low-risk active substance.

29

In Article 23—

a

in paragraph 1—

i

for “paragraphs 2 to 6” in both places it occurs substitute “ this Article ”;

ii

in the first subparagraph, omit the second sentence;

b

in paragraph 2, omit “Community”;

c

in paragraph 3—

i

in the first subparagraph—

aa

omit “by a Member State or”;

bb

for “Commission” substitute “ the competent authority for the constituent territory in relation to which approval is sought ”;

ii

in the second subparagraph, in point (a) omit “Community”;

d

omit paragraph 4;

e

for paragraph 5 substitute—

5
Article 6 applies to the approval of a basic substance.
5A
Within the decision period following receipt of the application and accompanying information, the competent authority must decide to either—
a
approve the basic substance, subject to conditions or restrictions, as referred to in Article 6(1), where appropriate, or
b
refuse to approve the basic substance.
5B
In paragraph 5A, the “decision period” is—
a
where the competent authority obtains independent scientific advice in respect of the application, nine months;
b
otherwise, six months.
5C
In making a decision under paragraph 5A, the competent authority must have regard to—
a
the application and accompanying information,
b
where the competent authority considers it appropriate to obtain it, any independent scientific advice obtained,
c
where the conditions laid down in Article 7(1) of Regulation (EC) No 178/2002 of the European Parliament and of the Council are relevant, the precautionary principle, and
d
any other matters which the competent authority considers relevant to the competent authority's determination of the application.
5D
As soon as reasonably practicable after making a decision under paragraph 5A, the competent authority must—
a
notify the applicant and the other competent authorities in writing of that decision and the reasons for it, and
b
update the approvals register accordingly.
5E
Article 20A applies to an approval of a basic substance which is subject to a condition in accordance with Article 6(1)(f) as it applies to an approval of an active substance.
5F
The Secretary of State may make a decision under paragraph 5A instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F66c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5G
Where the Secretary of State makes a decision in accordance with paragraph 5F, a reference in paragraphs 5A to 5D to the competent authority is to be read as a reference to the Secretary of State.

f

omit paragraph 6.

30

After Article 23 insert—

Article 23AReview of basic substance approval
1
A competent authority may review the approval of a basic substance at any time.
2
A competent authority must review the approval of a basic substance where—
a
the competent authority has received and assessed confirmatory information in accordance with Article 20A (as applied by Article 23(5E));
b
further information required in accordance with a condition under Article 6(1)(f) has not been provided within the period specified in that condition.
3
Where the competent authority considers that there are indications that the substance no longer satisfies the criteria provided for in Article 23(1) to (3), the competent authority must inform the other competent authorities and the interested party referred to in Article 23(3) accordingly, setting a period for the submission of comments.
4
The competent authority may obtain independent scientific advice, where the competent authority considers it appropriate to do so.
5
Where the competent authority concludes that, having considered comments received during the period set in accordance with paragraph 3 and any other information or matters that the competent authority considers important and relevant to the review, the substance no longer satisfies the criteria provided for in Article 23(1), the competent authority must decide to either—
a
amend the conditions of the approval, or
b
withdraw the approval.
6
As soon as reasonably practicable after making a decision under paragraph 5, the competent authority must—
a
notify the other competent authorities and the interested party referred to in Article 23(3) in writing of the decision and the reasons for it, and
b
update the approvals register accordingly.
7
The Secretary of State may review an active substance under paragraph 1 or 2 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F24c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
8
Where the Secretary of State reviews an active substance in accordance with paragraph 7, a reference in paragraphs 3 to 6 to the competent authority is to be read as a reference to the Secretary of State.

31

In Article 24—

a

in paragraph 1—

i

in the first sentence, omit “, for a period not exceeding seven years,”;

ii

omit the second sentence;

b

in paragraph 2, omit the second sentence.

32

Omit Article 25(3).

33

After Article 25 insert—

Article 25ASafeners and synergists on the market on or before 14th June 2011
1
A safener or synergist is deemed to be approved for the purposes of this Regulation in each constituent territory if on or before 14th June 2011 it was—
a
held for the purpose of sale within the European Union, an EEA state or the United Kingdom, including being offered for sale or other form of transfer, whether free of charge or not;
b
sold, distributed or otherwise transferred within the European Union, an EEA state or the United Kingdom, but not including return to the previous seller; or
c
released for free circulation into the territory of the European Union, an EEA state or the United Kingdom.
2
For the purposes of paragraph 1, “the European Union” does not include the Republic of Croatia.
3
A safener or synergist is deemed to be approved in accordance with paragraph 1 in a constituent territory until—
a
where an application for approval of that safener or synergist is received in accordance with Article 7 (as applied by Article 25(2)), the date on which a decision is made by the competent authority for that constituent territory or the Secretary of State in accordance with Article 13 (as applied by Article 25(2));
b
otherwise, the earliest of the following dates—
i
the date on which the competent authority or the Secretary of State decides to withdraw approval of the safener or synergist for that constituent territory in accordance with Article 21 as applied by paragraph 4;
ii
the date on which the first regulations made under Article 8(4)(a) in respect of safeners or synergists (as the case may be) which apply to that constituent territory come into force.
4
Article 21 applies to a safener or synergist deemed to be approved in accordance with paragraph 1 as if—
a
a reference to an active substance were a reference to that safener or synergist;
b
paragraph 2 were omitted;
c
in paragraph 3—
i
in point (a), the words from “or the assessment” to “Article 20A,” were omitted;
ii
point (b) (and the “or” immediately preceding it) were omitted;
d
in paragraph 5, for “or (b) apply” there were substituted “ applies ”;
e
paragraph 8(b) (and the “and” immediately preceding it) were omitted;
f
in paragraph 9, in the words before point (a) “or 2” were omitted.

34

In Article 27—

a

in paragraph 2, for the words from “in Annex III” to the end substitute “ on the unacceptable co-formulants register ”;

b

in paragraph 3—

i

for the first sentence substitute—

A competent authority may review co-formulants which are not accepted in the competent authority's constituent territory for inclusion in a plant protection product at any time.

ii

in the second sentence—

aa

for “It” substitute “ The competent authority ”;

bb

for “Member States” substitute “ the other competent authorities ”;

c

omit paragraph 4;

d

for paragraph 5 substitute—

5
The appropriate authority may, by regulations, make provision necessary for the implementation of this Article.

35

After Section 3, insert—

SECTION 4Registers
Article 27AApprovals register
1
The competent authorities must jointly establish and maintain a register of active substances, safeners, synergists, low-risk active substances, basic substances and candidates for substitution approved in accordance with this Regulation.
2
The entry on the register for each substance must contain the following information—
a
the common name and identification numbers of the substance;
b
the IUPAC name of the substance, where available;
c
the minimum purity of the substance;
d
in respect of each constituent territory to which the entry relates—
i
whether the substance has been approved as an active substance, safener, synergist, low-risk active substance, basic substance or candidate for substitution;
ii
the date of the approval decision;
iii
except in relation to approved basic substances, the expiration date of approval;
iv
information on any specific provisions, conditions or requirements in respect of the approved substance.
3
The register must contain a search facility.
4
The competent authorities must jointly make the register available for inspection by the public on a website maintained by one or more of the competent authorities.
Article 27BUnacceptable co-formulants register
1
The competent authorities must jointly establish and maintain a register of co-formulants which are not acceptable for inclusion in a plant protection product in accordance with Article 27.
2
The entry on the register for each co-formulant must contain the following information—
a
the common name of the co-formulant;
b
the IUPAC name of the co-formulant (where available);
c
the CAS number of the co-formulant (where available);
d
the EC number of the co-formulant (where available);
e
in respect of each constituent territory to which the entry relates—
i
the date of the decision that the co-formulant was not acceptable for inclusion in a plant protection product;
ii
the sunset date for the co-formulant;
iii
any conditions of restriction relating to the co-formulant;
iv
any other information regarding the co-formulant that the competent authority considers relevant.
3
The register must contain a search facility.
4
The competent authorities must jointly make the register available for inspection by the public on a website maintained by one or more of the competent authorities.

in point (g), for “all Member States” substitute “ F94Great Britain ”;

vi

in point (i), after “modified” insert “ in relation to the constituent territory of authorisation ”;

b

in paragraph 3, for “zone” substitute “ areas of F22Great Britain ”;

c

omit paragraphs 4 and 5;

d

in paragraph 6—

i

for the first subparagraph substitute—

a
The appropriate authority may, by regulations, prescribe uniform principles for the evaluation and authorisation of plant protection products.

F817

After paragraph 4 insert—

5
For the purposes of paragraph 4(c), Directive 2009/128/EC is to be read as if—
a
Article 3(10)(b) were omitted;
b
in Article 14—
i
obligations on Member States were obligations on the competent authorities;
ii
paragraph 3 were omitted.

8

In Article 32(1), in the second subparagraph—

a

after “approval” insert “ in the constituent territory of authorisation ”;

b

at the end, insert “ in the constituent territory of authorisation ”.

9

In Article 33—

a

for paragraph 1, substitute—

1
An applicant or a representative of the applicant may apply to the competent authority for authorisation to place a plant protection product on the market in a constituent territory.
1A
An applicant or a representative of the applicant may apply to the competent authority which granted an authorisation to amend that authorisation.

b

in paragraph 2—

i

in point (a), for the words from “in each zone” to “Member States where” substitute “ and the competent authorities to whom ”;

ii

omit point (b);

iii

in point (c), for “in a Member State” substitute “ by a competent authority ”;

iv

in point (d), for “Member State” substitute “ competent authority ”;

c

in paragraph 4, in the third subparagraph—

i

for “Member State” substitute “ competent authority ”;

ii

after “application” insert “ (see Article 35) ”;

d

for paragraph 5 substitute—

5
Where permitted by the competent authority, the applicant may submit an application in a language other than English.

e

in paragraph 6, for “Member State” substitute “ competent authority ”.

10

In Article 34—

a

in paragraph 1—

i

for the words from “Member State” to “application is made” substitute “ competent authority examining the application ”;

ii

at the end insert “ , or where paragraph 3 applies ”;

b

in paragraph 2—

i

in point (a), after “declaration that” insert “ , in respect of each constituent territory to which the application relates, ”;

ii

in point (b), after “approved” insert “ in respect of each constituent territory to which the application relates ”;

iii

in point (c), for “concerned Member State” substitute “ competent authority examining the application ”;

c

after paragraph 2 insert—

3
This paragraph applies where another competent authority has the test and study reports concerned.
4
Where paragraph 3 applies—
a
the competent authority examining the application must request those reports from the competent authority which has those reports, and
b
the competent authority which has those reports must send them to the competent authority examining the application as soon as reasonably practicable.

11

For Article 35 substitute—

Article 35Competent authority examining the application
1
For the purposes of this Subsection “the competent authority examining the application” is the competent authority which receives the application under Article 33.
2
But a competent authority may examine an application on behalf of one or more of the other competent authorities (and consequently for the purposes of this Subsection is “the competent authority examining the application”) where—
a
each competent authority receives the same application;
b
each competent authority agrees which competent authority is to examine the application;
c
each active substance, safener or synergist in the plant protection product to which the application relates—
i
is approved in relation to the constituent territory of each competent authority, and the conditions of each approval are compatible with the proposed authorisation, and
ii
has an equivalent technical specification in relation to each constituent territory, where necessary as determined in accordance with Article 38;
d
any co-formulant in the plant protection product to which the application relates is not included on the unacceptable co-formulants register in relation to the constituent territory of each competent authority; and
e
any data requirements specified in regulations made under Article 8(4)(a) and (b), any uniform principles for evaluation and authorisation of plant protection products prescribed in regulations made under Article 29(6)(a) and any guidance relating to those requirements or principles are the same in relation to the constituent territory of each competent authority.
3
Where paragraph 2 applies in relation to an application—
a
the competent authority examining the application must inform the applicant that it is to examine the application;
b
the other competent authorities must —
i
not proceed to determine the application pending assessment by the competent authority examining the application;
ii
at the request of the competent authority examining the application, cooperate to ensure a fair division of the workload.

12

In Article 36—

a

in paragraph 1—

i

in the first subparagraph—

aa

in the first sentence, for “Member State” substitute “ competent authority ”;

bb

in the second sentence, for “It shall give all Member States in the same zone” substitute “ Where Article 35(2) applies in relation to an application, the competent authority examining the application must give the other competent authorities ”;

ii

in the second subparagraph—

aa

for “Article 29(6)” substitute “ Article 29(6)(a) ”;

bb

omit “in the same zone”;

iii

for the third subparagraph substitute—

Where Article 35(2) applies in relation to an application, the competent authority examining the application must make available its assessment to the other competent authorities.

b

in paragraph 2—

i

for “The Member States concerned” substitute “ Where Article 35(2) applies in relation to an application, the competent authorities which received that application ”;

ii

for “Member State” substitute “ competent authority ”;

c

in paragraph 3—

i

in the first subparagraph, for “Community” substitute “ retained EU ”;

ii

in the second subparagraph—

aa

for “Member State” in the first place it occurs substitute “ competent authority ”;

bb

omit “national”;

cc

for “a Member State” in the second place it occurs substitute “ that competent authority ”;

dd

after “its” insert “ constituent ”;

iii

in the third subparagraph—

aa

for “Member State” substitute “ competent authority ”;

bb

for “Commission” substitute “ other competent authorities ”;

iv

omit the fourth subparagraph.

13

In Article 37—

a

in paragraphs 1 and 3, for “Member State” in each place it occurs substitute “ competent authority ”;

b

in paragraph 3, in the first sentence, for the words from “it has received” to the end substitute “ the draft assessment report for that active substance is circulated in accordance with Article 12(1)(a) ”;

c

after paragraph 3 insert—

3A
Where Article 35(2) applies in relation to an application, the requirement in paragraph 3 to decide on the application within 6 months of the active substance being approved is to be read as a requirement to decide on the application within 6 months of the earliest date on which the active substance is approved by one of the competent authorities which received the application for authorisation.

d

in paragraph 4—

i

for “The other Member States concerned” substitute “ Where Article 35(2) applies in relation to an application, the competent authorities which received the application for authorisation ”;

ii

for “Member State” substitute “ competent authority ”.

14

For Article 38 substitute—

Article 38Assessment of equivalence under Article 29(1)(b)
1
This Article applies where it is necessary in relation to an application to establish for an active substance, safener or synergist whether a different source or, for the same source a change of the manufacturing process or location complies with Article 29(1)(b).
1A
Where this Article applies, equivalence—
a
may be assessed by a competent authority examining the application, where—
i
each of the other competent authorities examining the application consents to that competent authority assessing equivalence, and
ii
in relation to the active substance, safener or synergist for which equivalence is to be assessed, any data requirements specified in regulations made under Article 8(4)(a) and (b), any uniform principles for evaluation and authorisation of plant protection products prescribed in regulations made under Article 29(6)(a) and any guidance issued under Article 77 relating to those requirements or principles are the same in relation to the constituent territory of each competent authority examining the application;
b
otherwise, must be assessed by each competent authority examining the application.
1B
The applicant must submit all necessary data to each competent authority assessing equivalence.
2
A competent authority assessing equivalence must—
a
give the applicant the opportunity to submit comments,
b
prepare a report on the competent authority's conclusion on equivalence within 60 days from receiving the application, and
c
provide a copy of that report to—
i
the applicant, and
ii
where the assessment is undertaken in accordance with paragraph 1A(a), the other competent authorities examining the application.
3
Where an assessment is undertaken in accordance with paragraph 1A(a), a competent authority examining the application which does not agree with the conclusion in the report provided in accordance with paragraph 2(c)(ii) must notify the competent authority which assessed equivalence, the other competent authorities examining the application and the applicant, stating its reasons for not agreeing.
3A
Following a notification under paragraph 3, the competent authorities concerned must—
a
give the applicant the opportunity to submit comments, and
b
try to reach agreement on whether Article 29(1)(b) is complied with.
4
Article 29(1)(b) is deemed not to be complied with where the competent authorities concerned under paragraph 3A do not reach agreement within 45 days of the latest date on which a notification from a competent authority is communicated in accordance with paragraph 3.

15

In Article 39—

a

in paragraph 1—

i

in the words before point (a)—

aa

for “Member States” substitute “ A competent authority ”;

bb

after “application” insert “ it receives ”;

ii

in point (b), omit the words from “the format” to “Article 79(2);”;

iii

in point (c), for “Member State” substitute “ competent authority ”;

b

in paragraph 2—

i

for “Member States” in the first place it occurs substitute “ a competent authority ”;

ii

for “Member States, the Commission and the Authority” substitute “ competent authorities ”;

c

in paragraph 3, for “Member States, the Commission and the Authority” substitute “ the competent authorities ”;

d

omit paragraph 4.

16

In Subsection 3—

a

in the heading, at the beginning insert “ Ongoing applications for ”;

b

omit Article 40;

c

before Article 41 insert—

Article 40AApplication and interpretation
1
This Subsection applies where—
a
before F50IP completion day the holder of an authorisation of a plant protection product granted by a member State or EEA state in accordance with Article 29 as it had effect immediately before F50IP completion day had applied for—
i
authorisation of the same product in the United Kingdom in accordance with Article 40 as it had effect immediately before F50IP completion day , or
ii
authorisation of the same product for minor uses in accordance with Articles 40 and 51(7) as those Articles had effect immediately before F50IP completion day , and
b
immediately before F50IP completion day that application had not been determined.
2
In this Subsection—
a
a reference to an Article as it had effect immediately before F50IP completion day in relation to an EEA state is a reference to that Article as adapted by the EEA Agreement as it had effect immediately before F50IP completion day ;
b
“reference state” means the member State or EEA state referred to in paragraph 1(a).

d

in Article 41—

i

in paragraph 1—

aa

for “Member State” in the first place it occurs substitute “ competent authority ”;

bb

after “Article 40” insert “ as it had effect immediately before F34IP completion day ”;

cc

for “Member State examining the application” substitute “ reference state ”;

ii

after paragraph 1 insert—

1A
But where the application was for authorisation of minor uses in accordance with Article 51(7) as it had effect immediately before F34IP completion day , the competent authority must authorise such uses, except where—
a
Article 36(3) applies, or
b
the competent authority considers that those uses are not minor.

iii

in paragraph 2—

aa

in the words before point (a), for “paragraph 1, the Member State” substitute “ paragraphs 1 and 1A, the competent authority ”;

bb

in point (a), after “Article 40(1)” insert “ as it had effect immediately before F34IP completion day ”;

cc

in point (b), at the end insert “ or ”;

dd

omit point (c).

17

Article 42 is amended in accordance with paragraphs (18) to (20).

18

In paragraph 1—

a

in point (a)—

i

for “Member State” in the first place it occurs substitute “ state ”;

ii

for the words from “an official language” to the end substitute “ English or another language permitted by the competent authority ”;

b

in point (b), for “Member State” substitute “ state ”;

c

in point (c), for “when requested by the Member State” substitute “ as it had effect immediately before F31IP completion day , when requested by the competent authority ”;

d

in point (d), for “Member State” substitute “ state ”.

19

In paragraph 2—

a

for “Member State” substitute “ competent authority ”;

b

for “an application under Article 40” substitute “ the application ”.

20

For paragraph 3 substitute—

3
Where permitted by the competent authority, the applicant may submit an application in a language other than English.

21

After Subsection 3 insert—

Subsection 3AMutual recognition of authorisations within F69Great Britain
Article 42AMutual recognition
1
This Subsection applies where a plant protection product has been authorised by a competent authority in accordance with Article 29 (the “reference competent authority”).
2
The following persons may apply for an authorisation for the same plant protection product, the same use and under comparable agricultural practices within the constituent territory of another competent authority—
a
the holder of the authorisation granted by the reference competent authority;
b
an official or scientific body involved in agricultural activities or a professional agricultural organisation—
i
with the consent of the authorisation holder, or
ii
where consent is refused, with the consent of the competent authority to which the application is made on the grounds of public interest.
3
An applicant under paragraph 2(b) must demonstrate that the use of such a plant protection product is of general interest within the constituent territory of the competent authority.
4
An application may not be made under paragraph 2 where—
a
the plant protection product contains an active substance, safener, synergist, low-risk active substance, basic substance or candidate for substitution which is not approved in relation to the constituent territory of the other competent authority;
b
the plant protection product contains an active substance, safener, synergist, low-risk active substance, basic substance or candidate for substitution which is approved in relation to the constituent territory of the other competent authority, but—
i
the conditions of that approval are incompatible with the product to which the application relates, or
ii
the technical specification relating to that approval is not equivalent to the technical specification of the approval of the same substance, safener, synergist or candidate in relation to the constituent territory of the reference competent authority, where necessary as determined in accordance with Article 38;
b
the plant protection product contains a co-formulant which is entered on the unacceptable co-formulants register in relation to the constituent territory of the other competent authority; or
c
the relevant data requirements specified in regulations made under Article 8(4)(a) and (b), the relevant uniform principles for evaluation and authorisation of plant protection products prescribed in regulations made under Article 29(6)(a) or any guidance issued under Article 77 relating to those requirements or principles are not the same in relation to the constituent territory of each competent authority.
Article 42BAuthorisation
1
The competent authority to which an application under Article 42A(2) is submitted, having examined the application and the accompanying documents referred to in Article 42C(1), and as appropriate with regards to the circumstances in its constituent territory, must authorise the plant protection product concerned under the same conditions as the reference competent authority, except in accordance with paragraph 2 or 3.
2
The competent authority may authorise the plant protection product where it contains a candidate for substitution or a substance approved in accordance with Article 4(7).
3
Paragraphs 1 and 2 do not apply where Article 36(3) applies.
Article 42CProcedure
1
An application under Article 42A must be accompanied by the following—
a
a copy of the authorisation granted by the reference competent authority;
b
a formal statement that the plant protection product is identical to that authorised by the reference competent authority;
c
a complete or summary dossier as required in Article 33(3) when requested by the competent authority;
d
an assessment report of the reference competent authority containing information on the evaluation and decision on the plant protection product.
2
The competent authority to which an application under Article 42A is submitted must decide on the application within 120 days.

22

In Article 43—

a

in paragraph 2—

i

in the words before point (a)—

aa

after “approval” insert “ in relation to a constituent territory ”;

bb

after “product” insert “ authorised in that constituent territory ”;

cc

after “information” insert “ to the competent authority for that constituent territory ”;

ii

in point (d), for “out in the Regulation” substitute “ by the competent authority ”;

b

in paragraph 3—

i

the existing first subparagraph becomes point (a);

ii

in that point (a)—

aa

for “Member States” substitute “ The competent authority examining the application ”;

bb

for the words from “in the Regulation” to the end substitute “ on renewal of the approval of the active substance, safener or synergist ”;

iii

for the second subparagraph substitute—

b
The competent authority which examined the plant protection product application in accordance with Article 35(2) may coordinate the compliance check and assessment of the information submitted for all competent authorities which receive an application for renewal of authorisation for the same product, provided that the conditions in Article 35(2) apply in relation to the renewal application.

d

after paragraph 4 insert—

5
In paragraph 1, “environmental objectives”—
a
in relation to the Northumbria River Basin District, means the objectives referred to in the WFD Regulations as applied by regulation 5 of the Water Environment (Water Framework Directive) (Northumbria River Basin District) Regulations 2003 M5;
b
in relation to the Solway Tweed River Basin District, means the objectives as defined in regulation 2 of the Water Environment (Water Framework Directive) (Solway Tweed River Basin District) Regulations 2004 M6;
c
in relation to any other river basin district, within the meaning of the WFD Regulations, has the same meaning as in those regulations;
d
in relation to a river basin district in Scotland, means the objectives set under section 9(1)(a)(i) of the Water Environment and Water Services (Scotland) Act 2003 M7;
F8e
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6
In paragraph 4, the “conditions” in the constituent territory of a competent authority include—
a
any data requirements specified in regulations made under Article 8(4)(a) or (b) in relation to that constituent territory;
b
any uniform principles prescribed by regulations made under Article 29(6)(a) in relation to that constituent territory;
c
any guidance issued under Article 77 in relation to that constituent territory.
7
In this Article—
a
“river basin district” means any of the following—
i
the Northumbria River Basin District;
ii
the Solway Tweed River Basin District;
iii
a river basin district within the meaning of the WFD Regulations;
iv
in relation to Scotland, an area designated as a river basin district by order under section 4(1) of the Water Environment and Water Services (Scotland) Act 2003;
F8v
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
b
“the WFD Regulations” means the Water Environment (Water Framework Directive) (England and Wales) Regulations 2017 M8.

F6124

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

25

In Article 47

a

in paragraph 1(a), at the end insert “ in relation to the constituent territory of application ”;

b

in paragraph (3)—

i

in the first subparagraph, for “The Member State” substitute “ A competent authority ”;

ii

in the second and third subparagraphs, for “Member State” in both places it occurs substitute “ competent authority ”.

26

In Article 48—

a

30

In Article 52—

a

omit paragraphs 1 to 4;

b

before paragraph 5 insert—

4A
This Article applies to a parallel trade permit issued before F68IP completion day by the United Kingdom as the Member State of introduction in accordance with this Article as it had effect immediately before F68IP completion day , where immediately before F68IP completion day the validity of that permit had not expired.

c

in paragraph 5, in the second sentence—

i

for “the Commission shall” substitute “ the appropriate authority may ”;

ii

for “a Regulation” substitute “ regulations ”;

iii

for “Article 68” substitute “ Article 68(3) ”;

d

for paragraph 6 substitute—

6
The parallel trade permit is valid in relation to a constituent territory until the earlier of—
a
the date on which the authorisation of the reference product expires in relation to that constituent territory;
F103b
the date two years after the day after the day on which IP completion day falls.
6A
Paragraph 6B applies to a parallel trade permit where—
a
the authorisation holder of the reference product for that permit applies for a withdrawal of authorisation in accordance with Article 45(1), and
b
the requirements of Article 29 are still fulfilled in respect of the product to which that permit relates.
6B
Where this paragraph applies, the date of expiry of the reference product for the purposes of paragraph 6(a) is deemed to be the date on which the authorisation of the reference product would have expired if the application under Article 45(1) had not been made.
6C
In paragraphs 4 to 6B, “reference product” means the plant protection product which was already authorised in the United Kingdom prior to the application for the parallel trade permit under paragraph 1 of this Article as it had effect immediately before F7IP completion day , and to which the product to which that permit relates is identical in composition.

e

after paragraph 8, insert—

8A
In paragraph 8, “Member State of origin” means the member State or EEA state which was the Member State of origin in accordance with paragraph 1 of this Article as it had effect immediately before F5IP completion day , as adapted by the EEA agreement as it had effect immediately before F5IP completion day .

e

omit paragraph 5.

33

In Article 55—

a

the existing first and second paragraphs become paragraphs 1 and 2;

b

in that paragraph 2, omit the words from “, which shall apply” to the end;

c

after that paragraph 2 insert—

3
For the purposes of this Article, Article 14 of Directive 2009/128/EC is to be read as if—
a
obligations on Member States were obligations on the competent authorities;
b
paragraph 3 were omitted.

34

In Article 56—

a

in paragraph 1—

i

in the first subparagraph, for “the Member States” substitute “ each competent authority ”;

ii

in the fourth subparagraph, for “third” substitute “ other ”;

b

in paragraph 3—

i

in the first subparagraph—

aa

for “Member States” in the first place it occurs substitute “ competent authorities ”;

bb

for “the Member State” substitute “ where paragraph 3A applies, the competent authority ”;

cc

omit “within each zone”;

dd

for “Member States, belonging to the same zone” substitute “ competent authorities which granted authorisation for the plant protection product ”;

ii

in the second subparagraph—

aa

for “Member State” substitute “ competent authority ”;

bb

for “Member States and the Commission” substitute “ competent authorities ”;

c

after paragraph 3 insert—

3A
This paragraph applies where—
a
each competent authority which granted authorisation agrees which competent authority is to evaluate the information;
b
each active substance, safener or synergist in the plant protection product to which the information relates has the same conditions of approval in relation to the constituent territory of each competent authority concerned;
c
any data requirements specified in regulations made under Article 8(4)(a) and (b), any uniform principles for evaluation and authorisation of plant protection products prescribed by regulations made under Article 29(6)(a) and any guidance issued under Article 77 relating to those requirements or principles are the same in relation to the constituent territory of each competent authority concerned.

d

in paragraph 4, omit “of the Member States”.

35

In Article 57—

a

in paragraph 1—

i

in the words before point (a), for “Member States” substitute “ A competent authority ”;

ii

in point (e), for the words from “to Directive 1999/45/EC” to the end substitute “ with Regulation (EC) No 1272/2008 of the European Parliament and of the Council and any regulations made under Article 65(1A) ”;

b

omit paragraph 3.

Chapter 4I2506

1

Chapter 4 is amended as follows.

2

For Article 58 substitute—

Article 58Placing on the market and use of adjuvants
1
An adjuvant must not be placed on the market or used in a constituent territory unless it has been authorised in that territory in accordance with Schedule 2 to the Plant Protection Products Regulations 2011 M14 F86... .
2
The appropriate authority may, by regulations, make provision regarding the authorisation of adjuvants including (but not limited to) data requirements, notification, evaluation, assessment and decision making procedures.

in the words before point (a), for “Member States” substitute “ a competent authority ”;

ii

in point (a), omit “, adjuvant”;

c

after paragraph 3 insert—

4
In paragraph 1, “assessing competent authority” has the same meaning as in Subsection 2 of Section 1 of Chapter 2.

Chapter 6I1658

1

Chapter 6 is amended as follows.

2

In Article 63(3), for “Directive 2003/4/EC of the European Parliament and of the Council of 28 January 2003 on public access to environmental information M15” substitute “ the Environmental Information Regulations 2004 M16 or the Environmental Information (Scotland) Regulations 2004 M17 ”.

Chapter 7I3559

1

Chapter 7 is amended as follows.

2

In Article 64(3)—

a

for “Article 9 of Directive 1999/45/EC” substitute “ Article 35 of Regulation (EC) No 1272/2008 of the European Parliament and of the Council ”;

b

for “Directive” in the second place it occurs substitute “ Regulation ”.

3

In Article 65—

a

for paragraph 1 substitute—

1
The labelling of plant protection products must include—
a
the classification, labelling and packaging requirements of Regulation (EC) No 1272/2008 of the European Parliament and of the Council, and
b
any requirements contained in regulations made under paragraph 1A which apply in relation to the constituent territory in which the product is to be placed on the market or used.
1A
The appropriate authority may, by regulations, specify additional requirements for the labelling of plant protection products, including (but not limited to) standard phrases for special risks and safety precautions which supplement the phrases provided for in Regulation (EC) No 1272/2008 of the European Parliament and of the Council.

b

in paragraph 2, for “Member States” substitute “ A competent authority ”;

c

omit paragraph 3.

4

In Article 66(3)—

a

for “Member States” substitute “ A competent authority ”;

b

for “Community” substitute “ retained EU ”.

omit “of the Member States”;

ii

for the words from “in accordance” to the end substitute “ for the purposes of establishing and maintaining risk indicators in accordance with Annex 4 to Directive 2009/128/EC ”;

d

omit paragraph 4.

F713

For Article 68 substitute—

Article 68Monitoring and controls
A competent authority shall publish by 31 August each year a report, for the previous year, on the scope and the outcome of the official controls performed in order to verify compliance with this Regulation.

Chapter 9I19211

1

Chapter 9 is amended as follows.

2

For Article 69 substitute—

Article 69Emergency measures
1
Where a competent authority is satisfied that the conditions in paragraph 2 are met, the competent authority may—
a
in the case of an active substance, safener or synergist approved in relation to its constituent territory—
i
amend the conditions of approval, or
ii
suspend approval;
b
in the case of a co-formulant, add that co-formulant to the unacceptable co-formulants register in relation to its constituent territory;
c
in the case of a plant protection product authorised in its constituent territory—
i
amend the authorisation for that product;
ii
suspend the authorisation for that product.
2
The conditions referred to in paragraph 1 are—
a
the approved active substance, safener, synergist, co-formulant or plant protection product is likely to constitute a serious risk to human or animal health or the environment, and
b
that risk cannot be contained satisfactorily by means of other measures taken by the competent authority.
3
In performing a function under paragraph 1, the competent authority may obtain independent scientific advice, where the competent authority considers it appropriate to do so.
4
As soon as reasonably practicable after acting in accordance with paragraph 1(a), (b) or (c), the competent authority must—
a
update the approvals register or unacceptable co-formulants register accordingly;
b
in relation to an amendment or suspension under paragraph 1(a), begin a review of the active substance, safener or synergist in accordance with Article 21 or that Article as applied by Article 25A(4);
c
in relation to a register addition under paragraph 1(b), begin a review of the co-formulant under Article 27(3);
d
in relation to an amendment or suspension under paragraph 1(c), begin a review of the plant protection product authorisation under Article 44.
5
An amendment or suspension under paragraph 1(a) expires upon the completion of the review described in paragraph 4(b).
6
A register addition under paragraph 1(b) expires upon the completion of the review described in paragraph 4(c).
7
An amendment or suspension under paragraph 1(c) expires upon the completion of the review described in paragraph 4(d).
8
Following the expiry of an amendment or suspension under paragraph 1(a), or a register addition under paragraph 1(b), the competent authority must update the approvals register or unacceptable co-formulants register accordingly.
9
The Secretary of State may perform a function under paragraph 1 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F49c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
10
Where the Secretary of State performs a function in accordance with paragraph 9, a reference to the competent authority in paragraphs 3 F1, 4 and 8 is to be read as a reference to the Secretary of State.

3

Omit Articles 70 and 71.

Chapter 10I15412

1

Chapter 10 is amended as follows.

2

Omit Article 72.

F293

In Article 73, for “the Member States” substitute “Great Britain”.

4

Omit Article 74.

5

In Article 75—

a

omit paragraphs 1 and 2;

b

in paragraph 3, for “Member States shall ensure that competent authorities have” substitute “ A competent authority must ensure that it has ”;

c

omit paragraphs 4 and 5.

6

For Articles 77 and 78 substitute—

Article 77Guidance documents
1
A competent authority may issue, amend or withdraw technical and other guidance documents relating to the implementation of this Regulation, including (but not limited to)—
a
guidance relating to the format of the summary or complete dossiers to be used for the purposes of Article 8;
b
guidance relating to the format of the draft assessment report for the purposes of Article 11;
c
guidance relating to the format of the assessment for the purposes of Article 36;
d
guidance regarding the rules and procedure for the assessment of equivalence under Article 38;
e
guidelines on the coordination of compliance checks to be undertaken in accordance with Article 43(3);
f
guidance on the application of Article 54, including on—
i
the maximum quantities of plant protection products that may be released during experiments or tests;
ii
the minimum data to be submitted in accordance with Article 54(2);
g
guidance concerning the content of the application concerning micro-organisms, pheromones and biological products.
2
A competent authority must publish any guidance document issued or amended, or a notice specifying any guidance document withdrawn, under paragraph 1 in a manner which that competent authority considers appropriate.
3
Before issuing, amending or withdrawing a guidance document under paragraph 1 a competent authority may obtain independent scientific advice, where the competent authority considers it appropriate to do so.
4
The Secretary of State may issue, amend or withdraw a guidance document under paragraph 1 instead of a competent authority—
a
in relation to Wales, with the consent of the Welsh Ministers;
b
in relation to Scotland, with the consent of the Scottish Ministers;
F99c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
5
Where the Secretary of State issues, amends or withdraws a guidance document in accordance with paragraph 4, a reference in paragraphs 2 and 3 to the competent authority is to be read as a reference to the Secretary of State.
6
In complying with any obligation under this Regulation, a person or competent authority must have regard to any guidance issued in accordance with paragraph 1.
Article 78Amendments and implementing measures
The appropriate authority may by regulations—
a
amend the Annexes to take account of current scientific and technical knowledge;
b
make further provision as necessary for the implementation of this Regulation.
Article 78ARegulations
1
Regulations made by the Secretary of State or Welsh Ministers under this Regulation are to be made by statutory instrument.
2
For regulations made under this Regulation by the Scottish Ministers, see section 27 of the Interpretation and Legislative Reform (Scotland) Act 2010 M18.
F993
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4
A statutory instrument containing regulations made by the Secretary of State under this Regulation is subject to annulment in pursuance of a resolution of either House of Parliament.
5
A statutory instrument containing regulations made by the Welsh Ministers under this Regulation is subject to annulment in pursuance of a resolution of the National Assembly for Wales.
6
Regulations made by the Scottish Ministers under this Regulation are subject to the negative procedure (see section 28 of the Interpretation and Legislative Reform (Scotland) Act 2010).
F997
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
8
Such regulations may—
a
contain consequential, incidental, supplementary, transitional or saving provision (including provision amending, repealing or revoking enactments);
b
make different provision for different purposes.

7

Omit Article 79.

Chapter 11I16013

1

Chapter 11 is amended as follows.

2

For Article 80, substitute—

Article 80Existing transitional measures
1
The following application is taken to have been made under Article 7(1) on the date it was made—
Common Name, CIPAC Identification Number
Applicant
Date of application
Ethametsulfuron
CIPAC-No: 834
DuPont de Nemours GmbH
29^th June 2010
1A
For the determination of the application described in paragraph 1, this Regulation is to be read subject to the modifications in paragraphs 1B to 1F.
1B
Article 4(1) is to be read as if—
a
in the first subparagraph—
i
“in accordance with Annex II” were omitted;
ii
the words from “, taking into account” to “that Annex,” were omitted;
b
the second subparagraph were omitted.
1C
Article 4(2)(a) is to be read as if the words from “, taking into account” to “available,” were omitted.
1D
Article 4(3) is to be read as if—
a
point (a) were omitted;
b
in point (b), the words from “or consequences” to “effects are available;” were omitted;
c
points (c), (d) and (e)(iii) were omitted;
1E
Article 4(7) is to be ignored.
1F
Article 11(2) is to be read as if the third subparagraph were omitted.
1G
Anything done before F26IP completion day in relation to the application described in paragraph 1—
a
by the United Kingdom —
i
under Directive 91/414/EEC, as the member State described in Article 6 of that Directive;
ii
as the rapporteur Member State under Regulation 188/2011;
b
by the European Food Safety Authority under Directive 91/414/EEC or Regulation 188/2011,
is taken to have been done by the relevant competent authority as the assessing competent authority.
1H
If the application described in paragraph 1 is approved in accordance with Article 13—
a
Article 13(1) to (4) of Directive 91/414/EEC applies in relation to that approval for a period of 10 years beginning with the date of approval;
b
Regulation 544/2011 and Regulation 545/2011 apply in relation to that approval as if, in Article A1(1)(a) of each Regulation, for the words from “as it had effect” in the first place it occurs to the end there were substituted “ as read with Article 80(1) of that Regulation ”.
1I
In paragraph 1G—
a
“rapporteur Member State” has the meaning given by Article 2(1) of Regulation 188/2011;
b
the “relevant competent authority” is the Secretary of State.
2
Paragraphs 2A to 2E apply to an active substance—
a
included in Annex 1 to Directive 91/414/EEC;
b
approved in accordance with paragraph 1 of this Article as it had effect immediately before F26IP completion day .
2A
Article 13(1) to (4) of Directive 91/414/EEC applies—
a
for active substances covered by Article 8(2) of Directive 91/414/EEC, for a period of five years beginning with the date of the inclusion or approval of the active substance;
b
for active substances which were not on the market in the European Union, an EEA state or the United Kingdom on 26th July 1993, for a period of 10 years from the date of the inclusion or approval of the active substance.
2B
In paragraph 2A(b), “on the market” means any supply, whether in return for payment or free of charge, other than for storage followed by consignment from the territory of the European Union, an EEA state or the United Kingdom or disposal.
2C
In paragraphs 2A(b) and 2B, the “European Union” does not include the Republic of Croatia.
2D
Regulation 544/2011 applies to the active substance, and is to be read as if, in Article A1(1) of that Regulation—
a
point (a) were omitted;
b
for F70point (c)(i) there were substituted—
i
described in Article 80(2) of Regulation (EC) No 1107/2009, and
2E
Regulation 545/2011 applies to the active substance, and is to be read as if, in Article A1(1) of that Regulation—
a
point (a) were omitted;
b
in F37point (c)(ii), for “to which point (a) applies” there were substituted “ described in Article 80(2) of Regulation (EC) No 1107/2009 ”.
2F
In this Article—
a
“assessing competent authority” has the same meaning as in Subsection 2 of Section 1 of Chapter 2;
b
“Directive 91/414/EEC” means Council Directive 91/414/EEC concerning the placing of plant protection products on the market, as it had effect by virtue of paragraph 1 and 2 of this Article as those paragraphs had effect immediately before F26IP completion day , read in accordance with paragraph 2G;
c
“Regulation 188/2011” means Commission Regulation (EU) No 188/2011 laying down detailed rules for the implementation of Council Directive 91/414/EEC as regards the procedure for the assessment of active substances which were not on the market 2 years after the date of notification of that Directive as it had effect immediately before F26IP completion day;
d
“Regulation 544/2011” means Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances;
e
“Regulation 545/2011” means Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products.
2G
For the purposes of this Article, Article 13(1) to (4) of Directive 91/414/EEC is to be read as if—
a
a term used in those paragraphs which is defined in this Regulation has the meaning given in this Regulation;
b
in paragraph 1—
i
in the words before point (a), for “Without prejudice to Article 10, Member States” there were substituted “ A competent authority ”;
ii
in point (a), for “Annex III” there were substituted “ Regulation 545/2011 ”;
iii
in point (b), for “Annex II” there were substituted “ Regulation 544/2011 ”;
c
in paragraph 3—
i
for “Member States” there were substituted “ a competent authority ”;
ii
for “Annex II” there were substituted “ Regulation 544/2011 ”;
iii
in point (b), for the words from “two years” to the end there were substituted “ by 26th July 1993 ”;
iv
point (c) (and the “or” immediately preceding it) were omitted;
v
in point (d), for “paragraphs 3(b) and (c)” there were substituted “ paragraph 3(b) ”;
d
in paragraph 4—
i
for “Member States” there were substituted “ a competent authority ”;
ii
for “Annex III” there were substituted “ Regulation 545/2011 ”;
iii
point (c) (and the “or” immediately preceding it) were omitted.

Common Name, CIPAC Identification Number	Applicant	Date of application
Ethametsulfuron CIPAC-No: 834	DuPont de Nemours GmbH	29^th June 2010

3

Omit Article 81.

4

In Article 83—

a

in the first paragraph—

i

omit “by the Acts listed in Annex V”;

ii

omit the words from “, without prejudice” to the end;

b

in the second paragraph, omit “in other Community legislation, such as Regulation (EC) No 1782/2003,”.

5

Omit Article 84.

6

After Article 84, omit the words from “This Regulation” to “all Member States”.

AnnexesI22914

1

The Annexes are amended as follows.

2

Omit Annex 1.

3

In Annex 2—

a

in point 1.1, for “rapporteur Member State and the Authority” substitute “ assessing competent authority ”;

b

in point 1.2, for “Authority and the rapporteur Member State” substitute “ assessing competent authority ”;

c

after point 1.2 insert—

1.2A. In this Annex, “the assessing competent authority” has the meaning given by Article 7(1C) or 15(1A) as the case may be.

Article 1Scope
1
This Regulation lays down the procedure for the determination of the existing renewal application by the relevant competent authority as assessing competent authority.
2
The “existing renewal application” is the application for the renewal of the approval of the active substance famoxadone which—
a
was made to the United Kingdom as rapporteur Member State in accordance with Article 4 as it had effect immediately before F45IP completion day , and
b
is taken as being made under this Regulation and Article 15(1) of Regulation (EC) No 1107/2009 on the date on which it was made.
3
Anything done under this Regulation as it had effect immediately before F45IP completion day in relation to the existing renewal application—
a
by the United Kingdom as rapporteur Member State;
b
by the European Food Safety Authority;
is taken to have been done by the relevant competent authority as the assessing competent authority.
4
In this Article—
a
“rapporteur Member State” has the meaning given in Article 2(c) as it had effect immediately before F45IP completion day ;
b
the “relevant competent authority” is the Secretary of State.

3

In Article 2—

a

for point (b) substitute—

b
‘applicant’ means the producer who made the existing renewal application;

b

omit points (c) to (f);

c

after point (f) insert—

g
‘Regulation (EC) No 1107/2009’ means Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market;
h
‘assessing competent authority’ has the meaning given by F39Article 15(1A) of Regulation (EC) No 1107/2009;
i
‘existing renewal application’ has the meaning given by Article 1(2).

4

After Article 2 insert—

Article 2ADetermination of existing renewal application
1
Where the assessing competent authority considers that additional data from the applicant is necessary to finalise the relevant conclusion, the assessing competent authority may set a period of up to one month for the applicant to supply that data.
2
The assessing competent authority must notify the other competent authorities—
a
as to the data received in accordance with paragraph 1, or
b
where no data is received during the period described in paragraph 1.
3
On request from a competent authority, the assessing competent authority must provide a copy of data received in accordance with paragraph 1.
4
The assessing competent authority must send the other competent authorities a finalised conclusion as soon as reasonably practicable after the conclusion is finalised.
5
Article 20 of Regulation (EC) No 1107/2009 applies to the determination of an existing renewal application, and for the purpose of that Article an existing renewal application is taken to relate to each constituent territory.
6
In paragraph 1, “relevant conclusion” means the conclusion of the European Food Safety Authority in respect of the existing renewal application, delivered in accordance with the second subparagraph of Article 16(2) as it had effect immediately before F85IP completion day .
7
In this Article, “competent authority” and “constituent territory” have the meanings given in Article 3A of Regulation (EC) No 1107/2009.

5

Omit Articles 3 to 21.

6

After Article 21, omit the words from “This Regulation” to “Member States”.

7

Omit Annexes 1 and 2.

Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substancesI10016

1

Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances is amended as follows.

2

Before Article 1, insert—

Article A1Scope and interpretation
1
This Regulation applies in relation to—
a
an application under Article 7 of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market as it had effect immediately before F40IP completion day where—
i
paragraph 6 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 applies to that application, and
ii
on or before 31st December 2013 dossiers were submitted in accordance with Article 8(1) and (2) of Regulation (EC) No 1107/2009 as it had effect immediately before F40IP completion day;
b
an application under Article 15 of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market as it had effect immediately before F40IP completion day where—
i
paragraph 7 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 applies to that application, and
ii
on or before 31st December 2013 dossiers were submitted in accordance with Article 9 of Commission Regulation (EU) No 1141/2010 laying down the procedure for the renewal of the inclusion of a second group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances as it had effect immediately before F40IP completion day;
c
an application for authorisation of a plant protection product, as referred to in Article 28 of Regulation (EC) No 1107/2009, which was submitted before 31st December 2015, F89as regards the submission of data concerning an active substance—
i
to which point (a) or (b) applies, or
ii
for which approval has not been renewed in accordance with Article 14 of Regulation (EC) No 1107/2009 or Commission Implementing Regulation (EU) No 844/2012 setting out the provisions necessary for the implementation of the renewal procedure for active substances, whether before or after F40IP completion day.
2
Paragraph 1(b) does not apply where the applicant for the authorisation notifies the competent authority in writing when submitting the application that the data requirements of Commission Regulation (EU) No 283/2013 setting out the data requirements for active substances apply instead.
3
Paragraph 4 applies where Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products.
4
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 545/2011, or a specified part of Commission Regulation (EU) No 545/2011, is to be read in relation to the application as a reference to Commission Regulation (EU) No 284/2013, or the equivalent part of Commission Regulation (EU) No 284/2013 (as the case may be).

3

Omit Article 2.

4

After Article 2, omit the words from “This Regulation shall” to “Member States”.

5

In the Annex—

a

in the Introduction—

i

in point 1.2, for the words from “the entry” to “Annex,” substitute “ 14th June 2011 ”;

ii

in point 1.3, for “Member States” substitute “ the competent authority ”;

iii

in point 1.6, for “Council Directive 86/609/EECM19” substitute “ the Animals (Scientific Procedures) Act 1986 M20 ”;

iv

in point 2.1, after “laid down in” insert “ Annex 1 to ”;

v

in point 2.2, in the first paragraph—

aa

for “Member States” substitute “ the competent authority ”;

bb

after “their” insert “ constituent ”;

vi

in point 2.3, in the first paragraph—

aa

for “Member States” substitute “ the competent authority ”;

bb

after “their” insert “ constituent ”;

cc

for “2 years after notification of the Directive 91/414/EECM21” substitute “ on or before 25th July 1993 ”;

b

in Part A—

F73i

in point 1.1, in the second paragraph, for the words from “the Member State” to “Commission” substitute “Great Britain”;

ii

in point 1.2, in the third sentence, for “the Commission and the Member States” substitute “ each competent authority which granted approval ”;

iii

in point 1.5, in the second sentence, omit “Member States or”;

iv

in point 1.9, in the second paragraph for “the Commission and the Member States” substitute “ each competent authority which granted approval ”;

v

in point 4.2.1, for “Member States” substitute “ competent authorities ”;

vi

in point 5.9, in the first paragraph, in the first sentence, after “the provisions of” insert “ the EU-derived domestic legislation which transposed M22 ”;

vii

in the Introduction to Section 6, in point (iii), for “the EU Guidelines for” substitute “ guidance issued under Article 77 of Regulation (EC) No 1107/2009 regarding ”;

viii

in point 6.10, omit “of the Member States”;

F59ix

in point 7.1, in the fourth paragraph, for “EU regions” substitute “regions of Great Britain”;

x

in point 7.1.1.2.1, under “Aerobic degradation”, under “Test conditions”, in the second paragraph, omit “EU”;

c

in Part B—

F98i

in point 1.1, in the second paragraph, for the words from “the Member State” to “Commission” substitute “Great Britain”;

ii

in point 1.2, for “the Commission and the Member States” substitute “ each competent authority which granted approval ”;

iii

in point 1.4.1, in the second paragraph for “the Commission and the Member States” substitute “ each competent authority which granted approval ”;

iv

in point 5.1.1, in the first paragraph, in the first sentence, after “the provisions of” insert “ the EU-derived domestic legislation which transposed ”;

F62v

in point 7.1.1, for “EU regions” substitute “regions of Great Britain”;

vi

in point 9, omit “of the Member States”.

Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection productsI34117

1

Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products is amended as follows.

2

Before Article 1, insert—

Article A1Scope and interpretation
1
This Regulation applies—
a
in relation to an application under Article 7 of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market as it had effect immediately before F9IP completion day where—
i
paragraph 6 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 applies to that application, and
ii
on or before 31st December 2013 dossiers were submitted in accordance with Article 8(1) and (2) of Regulation (EC) No 1107/2009 as it had effect immediately before F9IP completion day ;
b
in relation to an application under Article 15 of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market as it had effect immediately before F9IP completion day where—
i
paragraph 7 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 applies to that application, and
ii
on or before 31st December 2013 dossiers were submitted in accordance with Article 9 of Commission Regulation (EU) No 1141/2010 laying down the procedure for the renewal of the inclusion of a second group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances as it had effect immediately before F9IP completion day ;
c
in relation to an application for authorisation of a plant protection product, as referred to in Article 28 of Regulation (EC) No 1107/2009, where—
i
the application was submitted before 31st December 2015, and
ii
the plant protection product contains at least one active substance to which point (a) or (b) applies;
d
in relation to the renewal of the authorisation of a plant protection product in accordance with Article 43(2) of Regulation (EC) No 1107/2009 following the renewal (whether before or after F9IP completion day ) of an active substance in accordance with Commission Regulation (EU) No 1141/2010.
2
Paragraph 1(c) or (d) does not apply where the applicant for the authorisation notifies the competent authority in writing when submitting the application that the data requirements of Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products apply instead.
3
Paragraph 4 applies where Commission Regulation (EU) No 283/2013 setting out the data requirements for active substances applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances.
4
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 544/2011, or a specified part of Commission Regulation (EU) No 544/2011, is to be read in relation to that application as a reference to Commission Regulation (EU) No 283/2013, or the equivalent part of Commission Regulation (EU) No 283/2013 (as the case may be).

Commission Regulation (EU) No 546/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards uniform principles for evaluation and authorisation of plant protection products is amended as follows.

2

Before Article 1, insert—

Article A1Interpretation
1
Paragraph 2 applies where Commission Regulation (EU) No 283/2013 setting out the data requirements for active substances applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances.
2
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 544/2011, or a specified part of Commission Regulation (EU) No 544/2011, is to be read in relation to that application as a reference to Commission Regulation (EU) No 283/2013, or the equivalent part of Commission Regulation (EU) No 283/2013 (as the case may be).
3
Paragraph 4 applies where Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products.
4
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 545/2011, or a specified part of Commission Regulation (EU) No 545/2011, is to be read in relation to the application as a reference to Commission Regulation (EU) No 284/2013, or the equivalent part of Commission Regulation (EU) No 284/2013 (as the case may be).

xxiv

in point 2.8, for “Member States” in both places it occurs substitute “ Competent authorities ”.

Commission Regulation (EU) No 547/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards labelling requirements for plant protection productsI47319

1

Commission Regulation (EU) No 547/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards labelling requirements for plant protection products is amended as follows.

2

Before Article 1, insert—

Article A1Interpretation
1
Paragraph 2 applies where Commission Regulation (EU) No 283/2013 setting out the data requirements for active substances applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 544/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances.
2
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 544/2011, or a specified part of Commission Regulation (EU) No 544/2011, is to be read in relation to the application as a reference to Commission Regulation (EU) No 283/2013, or the equivalent part of Commission Regulation (EU) No 283/2013 (as the case may be).
3
Paragraph 4 applies where Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products applies in relation to an application by virtue of—
a
Article 1 of that Regulation, or
b
Article A1(2) of Commission Regulation (EU) No 545/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products.
4
Where this paragraph applies, a reference in this Regulation to Commission Regulation (EU) No 545/2011, or a specified part of Commission Regulation (EU) No 545/2011, is to be read in relation to the application as a reference to Commission Regulation (EU) No 284/2013, or the equivalent part of Commission Regulation (EU) No 284/2013 (as the case may be).

3

Omit Article 2.

4

After Article 2, omit the words from “This Regulation shall” to “Member States”.

5

In Annex 1—

a

in point (1)(c), in the first sentence, for “Article 10(2.3) of Directive 1999/45/EC of the European Parliament and of the Council” substitute “ Article 18(3) of Regulation (EC) No 1272/2008 of the European Parliament and of the Council ”;

b

for point (4) substitute—

4
A competent authority may make the placing of plant protection products on the market in its constituent territory subject to the additional labelling of the product in a language other than English.

6

In Annex 2—

a

in the words before point 1, in the first paragraph—

i

in the first sentence, for “Directive 1999/45/EC” substitute “ Regulation (EC) No 1272/2008 ”;

ii

in the second sentence, for “Directive” substitute “ Regulation ”;

b

for point 1.1 substitute—

1.1. Special risks related to humans (RSh)
RSh 1
— Toxic by eye contact.
RSh 2
— May cause photosensitisation.
RSh 3
— Contact with vapour causes burns to skin and eyes and contact with liquid causes freezing.

c

in point 2.1, for “risk phrases R34 or R35, as set out in Directive 1999/45/EC” substitute “ hazard statement H314 in Regulation (EC) No 1272/2008 of the European Parliament and of the Council ”.

7

In Annex 3—

a

in the words before point 1, in the first paragraph—

i

in the first sentence, for “Directive 1999/45/EC” substitute “ Regulation (EC) No 1272/2008 ”;

ii

in the second sentence, for “Directive” substitute “ Regulation ”;

b

for point 1 substitute—

1
General provisions
All plant-protection products shall be labelled with the following phrase, which shall be supplemented by the text in parentheses, as appropriate:
SP 1
— Do not contaminate water with the product or its container (Do not clean application equipment near surface water/Avoid contamination via drains from farmyards and roads).

c

for points 2.1 to 2.4 substitute—

2.1 Safety precautions for operators (SPo)
General provisions
1
Competent authorities may identify suitable personal protective equipment for operators and prescribe specific elements of this equipment (e.g. coveralls, apron, gloves, sturdy shoes, rubber boots, face protection, face shield, tightly fitting glasses, hat, hood or respirator of a specified type). Such supplementary safety precautions are without prejudice to the standard phrases applicable according to Regulation (EC) No 1272/2008 of the European Parliament and of the Council.
2
Competent authorities may further identify the specific tasks which require particular protective equipment, such as mixing, loading or handling the undiluted product, applying or spraying the diluted product, handling recently treated materials like plants or soil or entering recently treated areas.
3
Competent authorities may add specifications of engineering controls, such as:
— a closed transfer system must be used when transferring the pesticide from the product container to the spray tank,
— the operator must work within a closed cabin (with an air conditioning/air filtration system) during spraying,
— engineering controls may replace personal protective equipment if they provide an equal or higher standard of protection.
Specific provisions
SPo 1
— After contact with skin, first remove product with a dry cloth and then wash the skin with plenty of water.
SPo 2
— Wash all protective clothing after use.
SPo 3
— After igniting the product, do not inhale smoke and leave the treated area immediately.
SPo 4
— The container must be opened outdoors and in dry conditions.
SPo 5
— Ventilate treated areas/greenhouses thoroughly/time to be specified/until spray has dried before re-entry.
2.2 Safety precautions related to the environment (SPe)
SPe 1
— To protect groundwater/soil organisms do not apply this or any other product containing (identify active substance or class of substances, as appropriate) more than (time period or frequency to be specified).
SPe 2
— To protect groundwater/aquatic organisms do not apply to (soil type or situation to be specified) soils.
SPe 3
— To protect aquatic organisms/non-target plants/non-target arthropods/insects respect an unsprayed buffer zone of (distance to be specified) to non-agricultural land/surface water bodies.
SPe 4
— To protect aquatic organisms/non-target plants do not apply on impermeable surfaces such as asphalt, concrete, cobblestones, railway tracks and other situations with a high risk of run-off.
SPe 5
— To protect birds/wild mammals the product must be entirely incorporated in the soil; ensure that the product is also fully incorporated at the end of rows.
SPe 6
— To protect birds/wild mammals remove spillages.
SPe 7
— Do not apply during the bird breeding period.
SPe 8
— Dangerous to bees./To protect bees and other pollinating insects do not apply to crop plants when in flower./Do not use where bees are actively foraging./Remove or cover beehives during application and for (state time) after treatment./ Do not apply when flowering weeds are present./ Remove weeds before flowering./Do not apply before (state time).
2.3 Safety precautions related to good agricultural practice (SPa)
SPa 1
— To avoid the build-up of resistance do not apply this or any other product containing (identify active substance or class of substances, as appropriate) more than (number of applications or time period to be specified).
2.4 Specific safety precautions for rodenticides (SPr)
SPr 1
— The baits must be securely deposited in a way so as to minimise the risk of consumption by other animals. Secure bait blocks so that they cannot be dragged away by rodents.
SPr 2
— Treatment area must be marked during the treatment period. The danger from being poisoned (primary or secondary) by the anticoagulant and the antidote against it should be mentioned.
SPr 3
— Dead rodents must be removed from the treatment area each day during treatment. Do not place in refuse F92bins or on rubbish tips.

d

in point 3.1. for the words from “Annex to Regulation (EU) No” to “products]” substitute “ Annex to Commission Regulation (EU) No 546/2011 ”;

e

in point 3.3, for “Member States” in both places it occurs substitute “ competent authorities ”.

Commission Implementing Regulation (EU) No 844/2012 setting out the provisions necessary for the implementation of the renewal procedure for active substances, as provided for in Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the marketI60320

1

Commission Implementing Regulation (EU) No 844/2012 setting out the provisions necessary for the implementation of the renewal procedure for active substances, as provided for in Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market is amended as follows.

2

In Article 1—

F79a

in paragraph 1—

i

for the first subparagraph substitute—

An application for the renewal of an approval of an active substance must be submitted by a producer of the active substance to a competent authority for a constituent territory in relation to which the active substance is approved (in this Regulation, the “assessing competent authority”) no later than three years before the expiry of the approval.

i

for “rapporteur Member State” in the first place it occurs substitute “assessing competent authority";

ii

for the words from “rapporteur Member State" in the second place it occurs to the end substitute “ assessing competent authority ”;

b

after paragraph 1 insert—

1A
The assessing competent authority must notify the other competent authorities as soon as reasonably practicable after receipt of the supplementary dossiers under paragraph 1.
1B
A competent authority which receives a notification under paragraph 1A may request in writing from the applicant a copy of supplementary dossiers, which the applicant must provide as soon as reasonably practicable.

b

in the second sentence, for the words from “co-rapporteur” to “Authority” substitute “ other competent authorities ”.

10

For Article 10 substitute—

Article 10Refusal of renewal where applications are inadmissible
Where all of the applications submitted for renewal of the approval of an active substance in relation to a constituent territory are inadmissible in accordance with Article 3(3) or 8(6), the competent authority for that constituent territory must refuse to renew approval of the active substance in accordance with Article 20(1)(b) of Regulation (EC) No 1107/2009 of the European Parliament and of the Council.

11

In Article 11—

a

in the heading, for “rapporteur Member State and the co-rapporteur Member State” substitute “ assessing competent authority ”;

b

in paragraph 1—

i

for “rapporteur Member State shall, after consulting the co-rapporteur Member State” substitute “ assessing competent authority must ”;

ii

for “Commission, with a copy to the Authority,” substitute “ other competent authorities ”;

c

omit paragraph 2(g) and (h);

d

in paragraphs 3 and 4, for “rapporteur Member State” substitute “ assessing competent authority ”;

e

in paragraph 5—

i

in the first sentence, for “rapporteur Member State” substitute “ assessing competent authority ”;

ii

omit the second sentence,

f

after paragraph 5 insert—

5A
The F8213 month period provided for in paragraph 1 is extended by any additional period set in accordance with paragraph 5.
5B
The additional period described in paragraph 5 must be for no more than 6 months and ceases at the earlier of—
a
the date on which the assessing competent authority receives the additional information;
b
the expiry of the additional period.

g

for paragraph 6 substitute—

6
The assessing competent authority may, as it considers appropriate—
a
obtain independent scientific advice;
b
consult with the other competent authorities.

h

in paragraph 8—

i

for the first subparagraph substitute—

When submitting the draft renewal assessment report to the other competent authorities, the assessing competent authority must require the applicant to notify the other competent authorities of the existence of any updated supplementary summary dossiers. Article 15(4) of Regulation (EC) No 1107/2009 applies to a notification under this paragraph as it applies to a notification under Article 15(3) of that Regulation.

aa

for “Committee for Risk Assessment” substitute “Agency” in both places it occurs;

bb

for “37(4)” substitute “37A(4)”;

cc

for “Authority” substitute “assessing competent authority” in the first place it occurs; and

dd

for the second sentence, substitute—

The assessing competent authority may obtain independent scientific advice where it considers it appropriate to do so.

i

in points 1.6 and 1.7, omit “European”;

ii

in point 1.10, for “Directive 2010/63/EU of the European Parliament and of the Council” substitute “ the Animals (Scientific Procedures) Act 1986 ”;

iii

in point 1.13, for “accepted by European Food Safety Authority, (the Authority)” substitute “ set out in guidance issued in accordance with Article 77 of Regulation (EC) No 1107/2009 ”;

iv

in point 2, omit “at national level”;

v

in point 3.1, after “laid down in” insert “ Annex 1 to ”;

vi

in point 3.2.3, for “the application of this Regulation” substitute “ 1st January 2014 ”;

vii

omit point 6;

b

in Part A—

i

in point 1.2, for “Commission, the Authority and the Member States” substitute “ competent authorities ”;

ii

in point 1.5, omit “Member States or”;

iii

in point 3.9, for “Council Directive 94/67/ECM28” substitute “ the EU-derived domestic legislation which transposed Directive 2010/75/EU of the European Parliament and of the Council on industrial emissions (integrated pollution prevention and control) M29 ”;

iv

in point 4.2, in the first paragraph, in point (a) for “Member States” substitute “ competent authorities ”;

v

in point 5.8.3, in the second paragraph for “Union” substitute “ national ”;

vi

in point 5.9, in the first paragraph, in the first sentence, after “prejudice to” insert “ the EU-derived domestic legislation which transposed ”;

vii

in point 6.3, under “Test conditions”—

aa

for the fourth paragraph substitute—

For the evaluation of residue behaviour and the setting of maximum residue levels (MRLs) according to Regulation (EC) No 396/2005, residues trials data relevant to the agricultural practices in the UK must be provided. The trials must correspond to the critical GAP and the production conditions (such as cultural practices, climatic conditions) must be comparable to the UK. Differences in agricultural production methods (for example outdoor versus indoor uses), seasons of production, and types of formulation shall be taken into account.

v

in point 8.6, in the fifth sentence, for “crop management (ICM)” substitute “ pest management (IPM) ”;

vi

in Section 9, in the first sentence, omit “of the Member States”.

Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the marketI58022

1

Commission Regulation (EU) No 284/2013 setting out the data requirements for plant protection products, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market is amended as follows.

2

In Article 1—

a

the existing text becomes paragraph 1;

b

after that paragraph insert—

2
Paragraph 1 does not apply where Regulation (EU) No 545/2011 applies (see Article A1 of that Regulation).

3

Omit Articles 2 to 5.

4

After Article 5, omit the words from “This Regulation” to “Member States”.

5

In the Annex—

a

in the Introduction—

i

in point 1.6, omit “European”;

ii

in point 1.8, for “Directive 2010/63/EU of the European Parliament and of the Council” substitute “ the Animals (Scientific Procedures) Act 1986 ”;

iii

in point 1.11, for “Union legislation” substitute “ retained EU law ”;

iv

in point 1.14, for “accepted by the European Food Safety Authority (the Authority)” substitute “ set out in guidance issued in accordance with Article 77 of Regulation (EC) No 1107/2009 ”;

v

in point 2, omit the second sentence;

vi

in point 3.1, after “laid down in” insert “ Annex 1 to ”;

vii

in point 3.2(g), for “in a Member State” substitute “ by at least one competent authority ”;

viii

in point 3.3—

aa

for “Member State” substitute “ competent authority ”;

bb

after “its” insert “ constituent ”;

ix

omit point 6;

b

in Part A—

i

in points 1.4.3 and 4.4, for “Union legislation” substitute “ retained EU law ”;

ii

in point 4.5.2, in the first paragraph, for “Directive 94/67/EC of the Council” substitute “ the EU-derived domestic legislation which transposed Directive 2010/75/EU of the European Parliament and of the Council on industrial emissions (integrated pollution prevention and control) ”;

iii

in points 7.1.7 and 7.1.8, omit “national”;

iv

in points 7.2.1.2 and 7.2.3.2, after “in accordance with” in the second place it occurs insert “ the EU-derived domestic legislation which transposed ”;

v

in point 9.1.1.2.2, in the fourth paragraph—

aa

omit the words from “being included” to “introduction”;

bb

omit “national”;

vi

in points 9.1.2.3 and 9.2.3, omit “national”;

vii

in point 9.2.4.1, in the second paragraph, omit “EU”;

viii

in point 9.2.4.2, omit “national”;

ix

in point 9.2.5—

aa

in the second paragraph, omit “EU”;

bb

in the fourth paragraph, omit “national”;

x

in points 9.4, 10.1.3, 10.2.2, 10.4.2.2, 10.6.3 and 10.6.4, omit “national” in each place it occurs;

c

in Part B—

i

in point 1.1, in the second paragraph, for “ F10the Member State in which the authorisation is being sought” substitute “ F51Great Britain ”;

ii

in point 1.4(ii), for “Directive 1999/45/EC of the European Parliament and of the Council” substitute “ Regulation (EC) No 1272/2008 ”;

iii

in point 6.5, in the eighth paragraph—

aa

for “Member State” in the first place it occurs substitute “ competent authority ”;

bb

for “territory of this Member State” substitute “ constituent territory of that competent authority ”;

iv

in points 7.1, 7.1.1 and 7.1.3, omit “Directive 1999/45/EC or”;

v

in Section 11, in the first paragraph, omit “of the Member States”.

PART 3Transferred functions from Directive 2009/128/EC of the European Parliament and of the Council establishing a framework for Community action to achieve the sustainable use of pesticides

Power to update references to Annexes to Directive 2009/128/EC in light of scientific and technical progressI15923

1

The appropriate authority may, by regulations, make provision for a reference to a relevant Annex to Directive 2009/128/EC of the European Parliament and of the Council establishing a framework for Community action to achieve the sustainable use of pesticides in any enactment to be read as a reference to that Annex as modified by the regulations.

2

But the appropriate authority may exercise the power in paragraph (1) only to the extent that the appropriate authority considers that it is appropriate to do so as a result of scientific and technical progress.

3

The appropriate authority may, by regulations, amend any enactment which makes provision corresponding to that made by a relevant Annex to Directive 2009/128/EC for the purposes of ensuring that the provision made by the enactment continues to correspond to that made by the Annex as modified by regulations made under paragraph (1).

4

The relevant Annexes to Directive 2009/128/EC are—

a

Annex 1 (training subjects referred to in Article 5 of Directive 2009/128/EC);

b

Annex 2 (health and safety and environmental requirements relating to the inspection of pesticide application equipment);

c

Annex 3 (general principles of integrated pest management);

d

Annex 4 (harmonised risk indicators).

5

In this regulation, “the appropriate authority” means—

a

for regulations applying in relation to England, the Secretary of State;

b

for regulations applying in relation to Wales, the Welsh Ministers;

c

for regulations applying in relation to Scotland, the Scottish Ministers;

d

for regulations applying in relation to Northern Ireland, the Department.

6

But the appropriate authority is the Secretary of State if consent is given by—

a

for regulations applying in relation to Wales, the Welsh Ministers;

b

for regulations applying in relation to Scotland, the Scottish Ministers;

c

for regulations applying in relation to Northern Ireland, the Department.

7

In this regulation, “the Department” means the Department of Agriculture, Environment and Rural Affairs in Northern Ireland.

RegulationsI31824

1

Regulations made by the Secretary of State or Welsh Ministers under regulation 23 are to be made by statutory instrument.

2

For regulations made under regulation 23 by the Scottish Ministers, see section 27 of the Interpretation and Legislative Reform (Scotland) Act 2010.

3

Any power to make regulations conferred on the Department under regulation 23 is exercisable by statutory rule for the purposes of the Statutory Rules (Northern Ireland) Order 1979.

4

A statutory instrument containing regulations made by the Secretary of State under regulation 23 is subject to annulment in pursuance of a resolution of either House of Parliament.

5

A statutory instrument containing regulations made by the Welsh Ministers under regulation 23 is subject to annulment in pursuance of a resolution of the National Assembly for Wales.

6

Regulations made by the Scottish Ministers under regulation 23 are subject to the negative procedure (see section 28 of the Interpretation and Legislative Reform (Scotland) Act 2010).

7

Regulations made by the Department under regulation 23 are subject to negative resolution within the meaning of section 41(6) of the Interpretation Act (Northern Ireland) 1954.

8

Such regulations may—

a

contain consequential, incidental, supplementary, transitional or saving provision (including provision amending, repealing or revoking enactments);

b

make different provision for different purposes.

9

In this regulation, “the Department” has the meaning given in regulation 23(7).

PART 4Consequential amendments, savings, transitional provisions and revocations

Amendment of Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals AgencyI2925

In Article 15 of Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, for paragraph 1 substitute—

1
The following are regarded as being registered, and the registration as completed, for manufacture or import for the use as a plant protection product and therefore as fulfilling the requirements of Chapters 1 and 5 of this Title—
a
active substances manufactured or imported for use in plant protection products only and included in the approvals register in relation to at least one constituent territory;
b
co-formulants manufactured or imported for use in plant protection products only and not included in the unacceptable co-formulants register in relation to the whole of the UK;
c
any substance in relation to which the applicant has been notified in accordance with Article 9(3) of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.
1A
In paragraph 1—
a
in point (a)—
i
“approvals register” means the register maintained in accordance with Article 27A of Regulation (EC) No 1107/2009;
ii
“constituent territory” has the meaning given by Article 3A of Regulation (EC) No 1107/2009;
b
in point (b), “unacceptable co-formulants register” means the register maintained in accordance with Article 27B of Regulation (EC) No 1107/2009.

Amendment of the Plant Protection Products Regulations 2011I626

1

The Plant Protection Products Regulations 2011 are amended as follows.

2

In regulation 10—

a

for paragraph (1) substitute—

1
A person must not place on the market or use in a constituent territory (“the relevant constituent territory”) seeds treated with a plant protection product, other than an appropriate plant protection product, or cause or permit another person to do so.
1A
Paragraph (1) does not apply in relation to seeds which a competent authority must not prohibit in accordance with Article 49 as read with paragraph 14 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019.

b

in paragraph (3), for the words from “plant” to the end, substitute “ an appropriate plant protection product, or seeds which a competent authority must not prohibit in accordance with Article 49 as read with paragraph 14 of Schedule 1 to the Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019. ”;

c

after paragraph (3) insert—

4
In this regulation, “appropriate plant protection product” means—
a
a plant protection product authorised in relation to the relevant constituent territory for use on such seeds, or
b
a plant protection product authorised in relation to another constituent territory for use on such seeds, where—
i
every active substance, low-risk active substance or candidate for substitution in that product is approved in relation to the relevant constituent territory, and
ii
every co-formulant in that product does not appear on the unacceptable co-formulants register in relation to the relevant constituent territory.

Saving: the Plant Protection Products Regulations 2011I25927

1

The amendments made to regulation 10 of the Plant Protection Products Regulations 2011 by regulation 26 do not affect—

a

any obligation or liability acquired, accrued or incurred before F19IP completion day;

b

any penalty, forfeiture or punishment incurred in respect of any offence committed before F72IP completion day; or

c

any investigation, legal proceeding or remedy in respect of (a) or (b) above.

2

Any penalty, forfeiture or punishment referred to in paragraph (1)(b) may be imposed as if regulation 26 had not come into force.

3

Any investigation, legal proceeding or remedy referred to in paragraph (1)(c) may be instituted, continued or enforced as if regulation 26 had not come into force.

Transitional provisionsI8228

Schedule 1 has effect.

Revocation of retained EU legislation and savingI33629

1

The retained EU legislation in Schedule 2 is revoked.

2

Despite paragraph (1), a grace period contained within an EU instrument listed in Schedule 2 which expires after F14IP completion day continues to have effect, and is treated as if it had been set by each competent authority in relation to its constituent territory in accordance with Article 21(6)(b) of Regulation (EC) No 1107/2009.

Revocation: EEA agreementI33930

In Annex 2 to the EEA agreement, in Chapter 15—

a

omit points 12g and 12k;

b

omit the adaptations in point 13;

c

omit points 13a and 13aa;

d

omit the adaptations in point 13e;

e

omit points 13g to 13zzzzzzzzn.

Robert Goodwill Minister of State Department of Environment, Food and Rural Affairs

SCHEDULE 1Transitional provisions

Regulation 28

PART 1Interpretation

InterpretationI2801

In this Schedule—

“Regulation (EU) No 844/2012” means Commission Implementing Regulation (EU) No 844/2012 setting out the provisions necessary for the implementation of the renewal procedure for active substances, as provided for in Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market;
“plant protection product” has the meaning given by Article 2(1) of Regulation (EC) No 1107/2009.

PART 2Active substances, basic substances, low-risk active substances and candidates for substitution

Existing approvals of active substances, etc.: generalI4122

1

An active substance, basic substance, low-risk active substance or candidate for substitution which is set out in an entry in a table in the Annex is deemed to have been approved by each competent authority in relation to its constituent territory under Article 13 of Regulation (EC) No 1107/2009 in accordance with sub-paragraphs 2(3) and 2(4).

F232

Sub-paragraph (1) does not apply to an entry in a table in the Annex for an approval which expired before IP completion day.

3

An active substance, basic substance, low-risk active substance or candidate for substitution to which sub-paragraph (1) applies is deemed to have been approved—

a

from the date of approval stated in the relevant entry in the Annex;

b

until the existing expiration date, except—

i

for a basic substance, or

ii

as provided for in sub-paragraph (4);

c

subject to the specific provisions stated in the relevant entry in the Annex as modified in accordance with paragraph 3.

4

Where the existing expiration date for an approval is F90on or before the date three years after the day after the day on which IP completion day falls , approval is taken instead to expire at the end of a period of three years beginning with the existing expiration date.

5

In this paragraph—

“the Annex” means the Annex to Commission Implementing Regulation (EU) No 540/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances as it had effect immediately before F53IP completion day ;
“existing expiration date” means the date for the expiration of approval stated in the relevant entry in the Annex.

Existing approvals: Annex modificationsI2663

1

For the purposes of paragraph 2(3)(c), the Annex is modified in accordance with this paragraph.

2

In the Annex—

a

a reference to Member States is to be read as a reference to competent authorities;

b

a reference to Article 29(6) of Regulation (EC) No 1107/2009 is to be read as a reference to Article 29(6)(a) of that Regulation;

c

a requirement on a notifier to submit, or on a member State to ensure that a notifier submits, further studies, data or information to the Commission, one or more member States or the Authority within a period of time which has expired before F53IP completion day is to be ignored;

d

a requirement on member States to inform the Commission in accordance with Article 38 of Regulation (EC) No 1107/2009 is to be ignored;

3

The entries in the table in Part A of the Annex are modified as follows—

a

in entry 46 (Cyazofamid), in the seventh column, in the second paragraph, in the second sentence, the second indent is to be read as if “especially for Northern European regions” were omitted;

b

in entry 173 (Difenoconazole), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The notifier must submit to each competent authority the information set out in point (d) within 2 years from the issuing of specific guidance.

F105c

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

d

in entry 176 (Lenacil), in the seventh column, Part B is to be read as if, in the fourth paragraph, in the second sentence, for “the Commission” there were substituted “ each competent authority ”;

e

in entry 210 (Abamectin), in the seventh column, in Part B, the fourth paragraph is to be read as if for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

f

in entry 211 (Epoxiconazole), in the seventh column, Part B is to be read as if, for the third paragraph there were substituted—

The notifier must submit to each competent authority further studies addressing the potential endocrine disrupting properties of epoxiconazole within two years after the adoption of the OECD test guidelines on endocrine disruption or, alternatively, the issuing of test guidelines set by the competent authority.

g

in entry 217 (Metazachlor), in the seventh column, Part B is to be read as if, in the fifth paragraph, for “the Commission” there were substituted “ each competent authority ”;

h

in entry 268 (Tebuconazole), in the seventh column, Part B is to be read as if for the second paragraph there were substituted—

The notifier must submit to each competent authority further information addressing the potential endocrine disrupting properties of tebuconazole within two years after the adoption of the OECD test guidelines on endocrine disruption or, alternatively, the issuing of test guidelines set by the competent authority.

F105i

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

j

in entry 282 (Chlorsulfuron), in the seventh column, Part B is to be read as if, in the fourth paragraph, for “the Commission” there were substituted “ each competent authority ”;

k

in entry 284 (Dimethachlor), in the seventh column, Part B is to be read as if, in the fifth paragraph, for “the Commission” there were substituted “ each competent authority ”;

l

in entry 289 (Triflusulfron), in the seventh column, Part B is to be read as if, in the third paragraph, for “the Commission” there were substituted “ each competent authority ”;

m

in entry 307 (Sulfuryl fluoride), in the seventh column, Part B is to be read as if, in the fourth paragraph—

i

for “the Commission, Member States and the Authority” there were substituted “ each competent authority ”;

ii

for “2017” there were substituted “ 2022 ”;

n

in entry 315 (Fenbuconazole), in the seventh column, Part B is to be read as if, for the sixth paragraph there were substituted—

The notifier must submit to each competent authority further information addressing the potential endocrine disrupting properties of F17fenbuconazole within two years after the adoption of the OECD test guidelines on endocrine disruption or, alternatively, the issuing of test guidelines set by the competent authority.

o

in entry 318 (Bromuconazole), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The notifier must submit to each competent authority further information addressing the potential endocrine disrupting properties of bromuconazole within two years after the adoption of the OECD test guidelines on endocrine disruption or, alternatively, the issuing of test guidelines set by the competent authority.

p

in entry 327 (Oryzalin), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (4) within six months of notification of a decision classifying oryzalin.

q

in entry 328 (Tau-fluvalinate), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority confirmatory information addressing the possible impact on the environment of the potential enantio-selective degradation in environmental matrices, within two years after the issuing of specific guidance.

r

in entry 335 (Fluometuron), in the seventh column, Part B is to be read as if—

i

in the third paragraph, in the words before point (a), for “the Commission” there were substituted “ each competent authority ”;

ii

for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (d) within six months of notification of a decision classifying fluometuron.

s

in entry 337 (Carboxin), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (h) within six months of notification of a decision classifying carboxin.

t

in entry 338 (Cyproconazole), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (e) within two years of the issuing of specific guidance.

u

in entry 344 (Diclofop), in the seventh column, Part B is to be read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (b) within two years of the issuing of a specific guidance document on evaluation of isomers mixtures.

v

in entry 348 (Paclobutrazol), in the seventh column, Part B is to be read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority—
a
the information set out in point (4) within two years after the adoption of the OECD test guidelines on endocrine disruption, and
b
the information set out in point (5) within two years after the issuing of specific guidance.

w

in entry 352 (Hexythiazox), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (d) within two years after the issuing of specific guidance.

x

in entry 354 (Flurochloridone), in the seventh column, Part B is to be read as if—

i

in the fourth paragraph, in the words before point (1), for “the Commission” there were substituted “ each competent authority ”;

ii

for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (4) within two years after the adoption of the OECD test guidelines on endocrine disruption.

4

The entries in the table in Part B of the Annex are modified as follows—

a

in entry 7 (Sprioxamine), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (a) within two years after the issuing of specific guidance.

b

in entry 10 (Tefluthrin), in the seventh column, Part B is to be read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a specific guidance document on evaluation of isomers mixture.

c

in entry 16 (Terbuthylazine), in the seventh column, Part B is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (4) within six months of the notification of the classification decision for terbuthylazine.

d

in entry 19 (Acrinathrin), in the seventh column, Part B is to be read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (4) within two years after the issuing of specific guidance.

e

in entry 20 (Prochloraz), in the seventh column, Part B is to be read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the adoption of the OECD test guidelines on endocrine disruption.

f

in entry 48 (Sedaxane), in the seventh column, Part B is to be read as if for the sixth paragraph there were substituted—

The notifier must submit to each competent authority the relevant information within six months of the notification of the classification decision for sedaxane.

g

in entry 49 (Emamectin), the seventh column is to be read as if for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the relevant information within two years after the issuing of a specific guidance document on evaluation of isomers mixtures.

h

in entry 51 (Fluopyram), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (2) within two years after the adoption of the OECD test guidelines on endocrine disruption.

i

in entry 55 (Penflufen), in the seventh column, Part B is to be read as if in the fourth paragraph for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

j

in entry 57 (Penthiopyrad), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The notifier must submit to each competent authority the relevant information within six months of the notification of the classification decision for penthiopyrad.

k

in entry 60 (Spirotetramat), the seventh column is to be read as if in the fourth paragraph—

i

for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

for “Community agreed test guidelines” there were substituted “ test guidelines set by the competent authority ”;

l

in entry 67 (Spinetoram), the seventh column is to be read as if in the fifth paragraph, for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

m

in entry 69 (Amisulbrom), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (5) within two years after the adoption of OECD test guidelines on endocrine disruption.

n

in entry 73 (Ipconazole), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority—
a
the information set out in point (c) of the fourth paragraph within two years after the issuing of a specific guidance document on evaluation of isomer mixtures, and
b
the information set out in point (d) of the fourth paragraph within two years after the adoption of OECD or national test guidelines on endocrine disruption.

o

in entry 80 (Meptyldinocap), the seventh column is to be read as if , for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (b) within two years after the issuing of specific guidance.

p

in entry 91 (Flupyradifurone), the seventh column is to be read as if , for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

q

in entry 97 (Pinoxaden), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The notifier must submit to each competent authority the relevant information within six months of the notification of the classification decision for pinoxaden.

r

in entry 99 (Cyantraniliprole), the seventh column is to be read as if for the fourth paragraph there were substituted—

The applicant must submit to each competent authority confirmatory information as regards the effect of water treatment processes on the nature of residues present in surface and groundwater, when surface water or groundwater are abstracted for drinking water within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

s

in entry 100 (Isofetamid), the seventh column is to be read as if—

i

in the fourth paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

t

in entry 104 (Thifensulfuron-methyl), the seventh column is to be read as if—

i

in the fourth paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (4) within six months of the notification of the classification decision for thifensulfuron-methyl.

F74u

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

v

in entry 107 (Iodosulfuron), the seventh column is to be read as if—

i

in the fourth paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (2) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

w

in entry 108 (Flazasulfuron) and entry 111 (Mesosulfuron), the seventh column is to be read as if for the fourth paragraph there were substituted—

The applicant must submit to each competent authority confirmatory information as regards the effect of water treatment processes on the nature of residues present in surface and groundwater within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

x

in entry 112 (Mesotrione), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

y

in entry 114 (Propoxycarbazone), the seventh column is to be read as if for the fourth paragraph there were substituted—

The applicant must submit to each competent authority confirmatory information as regards the effect of water treatment processes on the nature of residues present in drinking water within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

z

in entry 121 (Silthiofam), the seventh column is to be read as if—

i

in the fourth paragraph, in the words before point 1, for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

in the fifth paragraph—

aa

for “Commission” there were substituted “ competent authority ”;

bb

for the words from “one year” to the end there were substituted “ six months of the notification of the classification decision for F18Silthiofam ”;

aa

in entry 123 (Zoxamide), the seventh column is to be read as if, in the fourth paragraph—

i

The applicant must submit to each competent authority confirmatory information as regards the effect of water treatment processes on the nature of residues present in surface and groundwater, when surface water or ground water is abstracted for drinking water.
The applicant must submit the requested information within two years from the date of publication of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

kk

in entry 139 (Florpyrauxifen-benzyl), the seventh column is to read as if, for the fourth paragraph there were substituted—

The applicant must submit to each competent authority an updated assessment of the information submitted and, where relevant, further information to confirm the absence of endocrine activity in accordance with points 3.6.5 and 3.8.2 of Annex 2 to Regulation (EC) No 1107/2009 by 24 July 2021.

5

The entries in the table in Part E of the Annex are modified as follows—

a

in entry 4 (Benzovindiflupyr), the seventh column is to be read as if, for the fifth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

b

in entry 7 (Pendimethalin), the seventh column is to be read as if—

i

in the fifth paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

ii

for the sixth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (2) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

c

in entry 9 (Propyzamide), the seventh column is to be read as if—

i

in the fifth paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “ each competent authority ”;

F100ii

for the sixth paragraph there were substituted—

The applicant must submit to each competent authority the information set out in point (3) within two years after the issuing of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

F44d

in entry 11 (Methoxyfenozide), the seventh column is to be read as if, in the fifth paragraph, in the words before point 1, for “the Commission, the Member States and the Authority” there were substituted “each competent authority”.

F57e

in entry 12 (Alpha-cypermethrin), the seventh column is to be read as if—

i

in the third paragraph, in the words before point (1), for “the Commission, the Member States and the Authority” there were substituted “each competent authority”;

ii

for the fourth paragraph there were substituted—

The applicant must submit the information requested in point (1) by 31 March 2021; the information requested in point (2) within two years from the date of publication of a guidance document on evaluation of isomer mixtures; and the information requested in point (3) within two years from the date of publication of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater.

iii

for the fifth paragraph there were substituted—

For the information requested in point (4), the applicant must submit an updated assessment of the information already submitted and, where relevant, further information to confirm the absence of androgenic endocrine activity by 30 October 2021.

6

In this paragraph, “the Annex” has the meaning given in paragraph 2(5).

Existing approvals: supplementaryI3814

1

When implementing the uniform principles as referred to in Article 29(6)(a) of Regulation (EC) No 1107/2009 for a plant protection product which contains an active substance, basic substance, low-risk active substance or candidate for substitution to which paragraph 2(1) applies, the competent authority must take into account the conclusions of the review report on that substance or candidate, and in particular Appendices 1 and 2 of that report.

2

Each competent authority must make available on request a free copy of a review report for an active substance, basic substance, low-risk active substance or candidate for substitution to which paragraph 2(1) applies.

3

Sub-paragraph (2) does not apply—

a

to any confidential information within the meaning of Article 63 of Regulation (EC) No 1107/2009;

b

otherwise, from the earliest of the following—

i

the date on which the approval of that substance or candidate is renewed;

ii

the date on which the approval of that substance or candidate is withdrawn or expires.

Existing candidates for substitution under Commission Implementing Regulation (EU) 2015/408I1355

1

An active substance which immediately before F53IP completion day is set out in the Annex to Commission Implementing Regulation (EU) 2015/408 on implementing Article 80(7) of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market and establishing a list of candidates for substitution is taken to have been approved by each competent authority in relation to its constituent territory under Article 13 of Regulation (EC) No 1107/2009 as a candidate for substitution.

2

Sub-paragraph (1) does not apply for the purposes of applications for plant protection products—

a

which were submitted before 4th April 2018, where the plant protection product contains 8-hydroxyquinoline;

b

otherwise, which were submitted before 1st August 2015.

by the rapporteur Member State;

b

by the European Food Safety Authority under Article 10 or 12 of Regulation (EC) No 1107/2009 as it had effect immediately before F53IP completion day ;

is taken to have been done by the relevant competent authority as the assessing competent authority.

5

In sub-paragraphs (3) and (4), the “relevant competent authority” is the Secretary of State, subject to sub-paragraphs (6) to (8).

6

The Secretary of State may appoint another competent authority as the relevant competent authority for an application to which this paragraph applies with the agreement of that competent authority.

7

The relevant competent authority must notify the applicant following an appointment under sub-paragraph (6).

8

An appointment in accordance with sub-paragraph (6) does not affect anything done by the Secretary of State as assessing competent authority prior to appointment.

9

In this paragraph—

“assessing competent authority” has the same meaning as in Subsection 2 of Section 1 of Chapter 2 of Regulation (EC) No 1107/2009;
“rapporteur Member State” has the meaning given by Article 3(22) of Regulation (EC) No 1107/2009 as it had effect immediately before F53IP completion day .

Ongoing active substance renewal applicationsI4967

1

This paragraph applies in relation to an application for renewal of the approval of an active substance where—

a

before F53IP completion day , that application was submitted to the United Kingdom as rapporteur Member State or co-rapporteur Member State in accordance with Article 1 of Regulation (EU) No 844/2012 as it had effect immediately before F53IP completion day , and

b

immediately before F53IP completion day a Regulation adopted under Article 20(1) of Regulation (EC) No 1107/2009 as it had effect immediately before F53IP completion day in relation to that application has not entered into force.

2

An application in relation to which this paragraph applies is taken as being made under Article 1 of Regulation (EU) No 844/2012 on the date on which it was made, and the relevant competent authority is the assessing competent authority for that application.

3

Anything done before F53IP completion day in relation to an application to which this paragraph applies—

a

by the rapporteur Member State or the United Kingdom as co-rapporteur Member State;

b

by the European Food Safety Authority under Regulation (EU) No 844/2012 as it had effect immediately before F53IP completion day ;

is taken to have been done by the relevant competent authority as the assessing competent authority.

4

In sub-paragraphs (2) and (3), the “relevant competent authority” is the Secretary of State subject to sub-paragraphs (5) to (7).

5

The Secretary of State may appoint another competent authority as the relevant competent authority for an application to which this paragraph applies F33with the agreement of that competent authority.

6

The relevant competent authority must notify the applicant following an appointment under sub-paragraph (5).

7

An appointment in accordance with sub-paragraph (5) does not affect anything done by the Secretary of State as assessing competent authority prior to appointment.

8

In this paragraph—

“assessing competent authority” has the meaning given by F64Article 15(1A) of Regulation (EC) No 1107/2009;
“co-rapporteur Member State” means the co-rapporteur Member State for the active substance which is the subject of the application as set out in the third column in the Annex to Commission Implementing Regulation (EU) No 686/2012 as it had effect immediately before F53IP completion day;
“rapporteur Member State” means the rapporteur Member State for the active substance which is the subject of the application as set out in the second column in the Annex to Commission Implementing Regulation (EU) No 686/2012 as it had effect immediately before F53IP completion day.

Requirement to provide existing maximum residue level applications in support of new active substance approval or renewal applicationsI458

3

Where sub-paragraph (2)(a) applies to an application, anything done by the member State or EEA state in respect of the examination of the application before F53IP completion day is taken to have been done by a competent authority.

4

In this paragraph, a reference to an Article of Regulation (EC) No 1107/2009 as it had effect immediately before F53IP completion day in respect of an EEA state means that Article as adapted by the EEA agreement as it had effect immediately before F53IP completion day .

Requirement to provide existing maximum F2residue level applications in support of new plant protection product authorisation applicationsI45410

1

Sub-paragraph (2) applies where—

a

on or after F53IP completion day an application is made for authorisation of a plant protection product or amendment of such an authorisation in accordance with Article 33 of Regulation (EC) No 1107/2009, and

b

2

Where this sub-paragraph applies, the obligation in Article 33(3)(e) of Regulation (EC) No 1107/2009 to provide a copy of a relevant application for a maximum residue level F56as referred to in Article 7 of Regulation (EC) No 396/2005 is to be read as including F88an obligation to provide a copy of the application described in sub-paragraph (1)(b).

Assessment of equivalence under Article 38(1) of Regulation (EC) No 1107/2009 where active substance last approved before F53IP completion dayI20011

1

Sub-paragraph (2) applies where—

a

3

In sub-paragraph (1)(b) and (c), the reference to Article 56(3) of Regulation (EC) No 1107/2009 as it had effect immediately before F53IP completion day in relation to an EEA state means that Article as adapted by the EEA agreement as it had effect immediately before F53IP completion day .

PART 4Treated seeds

Treated seedsI28414

Commission Regulation (EEC) No 3600/92 laying down the detailed rules for the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I262

Commission Regulation (EC) No 933/94 laying down the active substances of plant protection products and designating the rapporteur Member States for the implementation of Commission Regulation (EEC) No 3600/92.

I4583

Commission Regulation (EC) No 491/95 amending Regulation (EEC) No 3600/92 and Regulation (EC) No 933/94, in particular with regard to the integration of the designated public authorities and the producers in Austria, Finland and Sweden in the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I4664

Commission Regulation (EC) No 2230/95 amending Regulation (EC) No 933/94 laying down the active substances of plant protection products and designating the rapporteur Member States for the implementation of Commission Regulation (EEC) No 3600/92.

I45

Commission Regulation (EC) No 1199/97 amending Regulation (EEC) No 3600/92 laying down the detailed rules for the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I4626

Commission Regulation (EC) No 1972/1999 amending Regulation (EEC) No 3600/92 laying down the detailed rules for the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I257

Commission Regulation (EC) No 451/2000 laying down the detailed rules for the implementation of the second and third stages of the work programme referred to in Article 8(2) of Council Directive 91/414/EEC.

I1198

Commission Regulation (EC) No 2266/2000 amending Regulation (EEC) No 3600/92 laying down the detailed rules for the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I3249

Commission Regulation (EC) No 703/2001 laying down the active substances of plant protection products to be assessed in the second stage of the work programme referred to in Article 8(2) of Council Directive 91/414/EEC and revising the list of Member States designated as rapporteurs for those substances.

I27910

Commission Regulation (EC) No 1490/2002 laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and amending Regulation (EC) No 451/2000.

I3311

Commission Regulation (EC) No 1044/2003 amending Regulations (EC) No 451/2000 and (EC) No 1490/2002.

I29312

Commission Regulation (EC) No 1336/2003 amending Regulation (EC) No 2076/2002 as regards the continued use of the substances listed in Annex II.

I42613

Commission Regulation (EC) No 771/2004 laying down transitional measures with regard to continued use of plant protection products containing certain active substances following the accession of new Member States to the European Union.

I34514

Commission Regulation (EC) No 835/2004 adapting Regulation (EC) No 2076/2002 and Decisions 2002/928/EC, 2004/129/EC, 2004/247/EC and 2004/248 as regards the continued use of certain active substances not included in Annex I to Directive 91/414/EEC, by reason of the accession of the Czech Republic, Estonia, Cyprus, Latvia, Lithuania, Hungary, Malta, Poland, Slovenia and Slovakia.

I23615

Commission Regulation (EC) No 1744/2004 amending Regulation (EC) No 1490/2002 as regards the replacement of a rapporteur Member State.

I21416

Commission Regulation (EC) No 1765/2004 amending Regulation (EC) No 2076/2002 as regards the continued use of the substances listed in Annex II.

I35417

Commission Regulation (EC) No 2229/2004 laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC.

I29018

Commission Regulation (EC) 1335/2005 amending Regulation (EC) No 2076/2002 and Decisions 2002/928/EC, 2004/129/EC, 2004/140/EC, 2004/247/EC and 2005/303/EC as regards the time period referred to in Article 8(2) of Council Directive 91/414/EEC and the continued use of certain substances not included in its Annex I.

I56219

Commission Regulation (EC) No 1980/2006 laying down transitional measures amending Regulation (EC) No 2076/2002 and Decisions 2001/245/EC, 2002/928/EC and 2006/797/EC as regards the continued use of certain active substances not included in Annex I to Directive 91/414/EC by reason of the accession of Bulgaria.

I6220

Commission Regulation (EC) No 2024/2006 laying down transitional measures derogating from Regulation (EC) No 2076/2002 and Decisions 98/270/EC, 2002/928/EC, 2003/308/EC, 2004/129/EC, 2004/141/EC, 2004/247/EC, 2004/248/EC, 2005/303/EC and 2005/864/EC as regards the continued use of plant protection products containing certain active substances not included in Annex I to Directive 91/414/EC by reason of the accession of Romania.

I35221

Commission Regulation (EC) No 647/2007 amending Regulation (EC) No 2229/2004 laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC.

I16922

Commission Regulation (EC) No 737/2007 on laying down the procedure for the renewal of the inclusion of a first group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances.

I41923

Commission Regulation (EC) No 1095/2007 amending Regulation (EC) No 1490/2002 laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and Regulation (EC) No 2229/2004 laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC.

I38324

Commission Regulation (EC) No 1313/2007 amending Regulations (EC) No 2076/2002 as regards the extension of the time period referred to in Article 8(2) of Council Directive 91/414/EEC with respect to metalaxyl and (EC) No 2024/2006 as regards the deletion of the derogation concerning metalaxyl.

I21225

Commission Regulation (EC) No 33/2008 laying down detailed rules for the application of Council Directive 91/414/EEC as regards a regular and an accelerated procedure for the assessment of active substances which were part of the programme of work referred to in Article 8(2) of that Directive but have not been included into its Annex I.

I53926

Commission Regulation (EC) No 416/2008 amending Regulation (EEC) No 3600/92 as regards the assessment of the active substance metalaxyl in the framework of Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I40927

Commission Regulation (EC) No 848/2008 amending Regulation (EC) No 2076/2002 and Decision 2003/565/EC as regards the time period provided for in Article 8(2) of Council Directive 91/414/EEC.

I24428

Commission Regulation (EU) No 78/2010 amending Regulation (EC) No 33/2008 as regards the scope and the period granted under the regular procedure to the Authority for the adoption of its conclusions concerning the inclusion of certain active substances in Annex I to Directive 91/414/EEC.

I17329

Commission Regulation (EU) No 114/2010 amending Regulation (EC) No 2229/2004 as regards the time period granted to EFSA for the delivery of its view on the draft review reports concerning the active substances for which there are clear indications that they do not have any harmful effects.

I41030

Commission Regulation (EU) No 741/2010 amending Regulations (EC) No 1490/2002 and (EC) No 2229/2004 as regards the date until which authorisations may continue to be in force at 31.12.2020 in cases where the notifier has submitted an application in accordance with the accelerated procedure under Regulation (EC) No 33/2008.

I36831

Commission Implementing Regulation (EU) No 540/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances.

I6632

Commission Implementing Regulation (EU) No 541/2011 amending Implementing Regulation (EU) No 540/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances.

I30133

Commission Implementing Regulation (EU) No 542/2011 amending Implementing Regulation (EU) No 540/2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances to take into account Directive 2011/58/EU amending Council Directive 91/414/EEC to renew the inclusion of carbendazim as active substance.

I27334

Commission Implementing Regulation (EU) No 702/2011 approving the active substance prohexadione, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I14135

Commission Implementing Regulation (EU) No 703/2011 approving the active substance azoxystrobin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I24636

Commission Implementing Regulation (EU) No 704/2011 approving the active substance azimsulfuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I14737

Commission Implementing Regulation (EU) No 705/2011 approving the active substance imazalil, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I60938

Commission Implementing Regulation (EU) No 706/2011 approving the active substance profoxydim, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I7539

Commission Implementing Regulation (EU) No 736/2011 approving the active substance fluroxypyr, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I11140

Commission Implementing Regulation (EU) No 740/2011 approving the active substance bispyribac, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I48641

Commission Implementing Regulation (EU) No 786/2011 approving the active substance 1-naphthylacetamide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/941/EC.

I14542

Commission Implementing Regulation (EU) No 787/2011 approving the active substance 1-naphthylacetic acid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/941/EC.

I47243

Commission Implementing Regulation (EU) No 788/2011 approving the active substance fluazifop-P, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011and Commission Decision 2008/934/EC.

I36344

Commission Implementing Regulation (EU) No 797/2011 approving the active substance spiroxamine, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I1745

Commission Implementing Regulation (EU) No 798/2011 approving the active substance oxyfluorfen, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/934/EC.

I28246

Commission Implementing Regulation (EU) No 800/2011 approving the active substance tefluthrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011and Commission Decision 2008/934/EC.

I7347

Commission Implementing Regulation (EU) No 806/2011 approving the active substance fluquinconazole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/934/EC.

I53548

Commission Implementing Regulation (EU) No 807/2011 approving the active substance triazoxide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I17149

Commission Implementing Regulation (EU) No 810/2011 approving the active substance kresoxim-methyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I12550

Commission Implementing Regulation (EU) No 820/2011 approving the active substance terbuthylazine, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/934/EC.

I24251

Commission Implementing Regulation (EU) No 942/2011 concerning the non-approval of the active substance flufenoxuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Decision 2008/934/EC.

I2252

Commission Implementing Regulation (EU) No 943/2011 concerning the non-approval of the active substance propargite, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Decision 2008/934/EC.

I52953

Commission Implementing Regulation (EU) No 974/2011 approving the active substance acrinathrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/934/EC.

I19354

Commission Implementing Regulation (EU) No 993/2011 approving the active substance 8-hydroxyquinoline, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I32555

Commission Implementing Regulation (EU) No 1022/2011 concerning the non-renewal of the approval of the active substance cyclanilide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I13856

Commission Implementing Regulation (EU) No 1045/2011 concerning the non-approval of the active substance asulam, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Decision 2008/934/EC.

I35657

Commission Implementing Regulation (EU) No 1078/2011 concerning the non-approval of the active substance propanil, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I15558

Commission Implementing Regulation (EU) No 1100/2011 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances dicamba, difenoconazole, imazaquin.

I1659

Commission Implementing Regulation (EU) No 1127/2011 concerning the non-approval of the active substance 2-naphthyloxyacetic acid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I44460

Commission Implementing Regulation (EU) No 1134/2011 concerning the non-renewal of the approval of the active substance cinidon-ethyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I51261

Commission Implementing Regulation (EU) No 1143/2011 approving the active substance prochloraz, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and Commission Decision 2008/934/EC.

I57262

Commission Implementing Regulation (EU) No 1372/2011 concerning the non-approval of the active substance acetochlor, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Decision 2008/934/EC.

I22563

Commission Implementing Regulation (EU) No 1381/2011 concerning the non-approval of the active substance chloropicrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Decision 2008/934/EC.

I16264

Commission Implementing Regulation (EU) No 87/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance clethodim.

I60465

Commission Implementing Regulation (EU) No 127/2012 amending Implementing Regulation (EU) No 540/2011 as regards an extension of the use of the active substance metazachlor.

I26866

Commission Implementing Regulation (EU) No 287/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance triflusulfuron.

I29167

Commission Implementing Regulation (EU) No 359/2012 approving the active substance metam, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I30368

Commission Implementing Regulation (EU) No 369/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances blood meal, calcium carbide, calcium carbonate, limestone, pepper and quartz sand.

I45569

Commission Implementing Regulation (EU) No 571/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances aluminium silicate, hydrolysed proteins and 1,4-diaminobutane (putrescine).

I41670

Commission Implementing Regulation (EU) No 578/2012 concerning the non approval of the active substance diphenylamine, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I571

Commission Implementing Regulation (EU) No 582/2012 approving the active substance bifenthrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I22372

Commission Implementing Regulation (EU) No 589/2012 approving the active substance fluxapyroxad, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I34973

Commission Implementing Regulation (EU) No 595/2012 approving the active substance fenpyrazamine, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I37274

Commission Implementing Regulation (EU) No 597/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances aluminium ammonium sulphate, fat distillation residues, repellents by smell of animal or plant origin/fish oil and urea.

I375

Commission Implementing Regulation (EU) No 608/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances denathonium benzoate, methyl nonyl ketone and plant oils/spearmint oil.

I16376

Commission Implementing Regulation (EU) No 637/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substances iron sulphate, repellents by smell of animal or plant origin/tall oil crude and repellents by smell of animal or plant origin/tall oil pitch.

I1377

Commission Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of active substances whose approval expires by 31 December 2018 at the latest.

I43978

Commission Implementing Regulation (EU) No 735/2012 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance potassium hydrogen carbonate.

I3979

Commission Implementing Regulation (EU) No 746/2012 approving the active substance Adoxophyes orana granulovirus, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I12280

Commission Regulation (EU) No 823/2012 derogating from Implementing Regulation (EU) No 540/2011 as regards the expiry dates of the approval of the active substances 2,4-DB, benzoic acid, beta-cyfluthrin, carfentrazone ethyl, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), cyazofamid, cyfluthrin, deltamethrin, dimethenamid-P, ethofumesate, ethoxysulfuron, fenamidone, flazasulfuron, flufenacet, flurtamone, foramsulfuron, fosthiazate, imazamox, iodosulfuron, iprodione, isoxaflutole, linuron, maleic hydrazide, mecoprop, mecoprop-P, mesosulfuron, mesotrione, oxadiargyl, oxasulfuron, pendimethalin, picoxystrobin, propiconazole, propineb, propoxycarbazone, propyzamide, pyraclostrobin, silthiofam, trifloxystrobin, warfarin and zoxamide.

I33881

Commission Implementing Regulation (EU) No 1037/2012 approving the active substance isopyrazam, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant production products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I27282

Commission Implementing Regulation (EU) No 1043/2012 approving the active substance phosphane, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I4383

Commission Implementing Regulation (EU) No 1197/2012 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances acetamiprid, alpha-cypermethrin, Ampelomyces quisqualis Strain: AQ 10, benalaxyl, bifenazate, bromoxynil, chlorpropham, desmedipham, etoxazole, Gliocladium catenulatum Strain: J1446, imazosulfuron, laminarin, mepanipyrim, methoxyfenozide, milbemectin, phenmedipham, Pseudomonas chlororaphis Strain: MA 342, quinoxyfen, S-metolachlor, tepraloxydim, thiacloprid, thiram and ziram.

I33584

Commission Implementing Regulation (EU) No 1237/2012 approving the active substance Zucchini Yellow Mosaic Virus – weak strain, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I18485

Commission Implementing Regulation (EU) No 1238/2012 approving the active substance Trichoderma asperellum (strain T34), in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I56686

Commission Implementing Regulation (EU) No 17/2013 approving the active substance Trichoderma atroviride strain I-1237, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I40787

Commission Implementing Regulation (EU) No 22/2013 approving the active substance cyflumetofen, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I54788

Commission Implementing Regulation (EU) No 175/2013 amending Implementing Regulation (EU) No 540/2011 as regards the withdrawal of the approval of the active substance didecyldimethylammonium chloride.

I9489

Commission Implementing Regulation (EU) No 187/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance ethylene.

I20990

Commission Implementing Regulation (EU) No 188/2013 approving the active substance mandipropamid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I59991

Commission Implementing Regulation (EU) No 190/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance sodium hypochlorite.

I28892

Commission Implementing Regulation (EU) No 200/2013 approving the active substance ametoctradin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I5393

Commission Implementing Regulation (EU) No 201/2013 amending Implementing Regulations (EU) No 788/2011 and (EU) No 540/2011 as regards an extension of the uses for which the active substance fluazifop-P is approved.

I24594

Commission Implementing Regulation (EU) No 350/2013 approving the active substance bixafen, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I53895

Commission Implementing Regulation (EU) No 355/2013 approving the active substance maltodextrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I55296

Commission Implementing Regulation (EU) No 356/2013 approving the active substance halosulfuron-methyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I42497

Commission Implementing Regulation (EU) No 365/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance glufosinate.

I17798

Commission Implementing Regulation (EU) No 366/2013 approving the active substance Bacillus firmus I-1582, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I199

Commission Implementing Regulation (EU) No 367/2013 approving the active substance Spodoptera littoralis nucleopolyhedrovirus, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I166100

Commission Implementing Regulation (EU) No 368/2013 approving the active substance Heliocoverpa armigera nucleopolyhedrovirus, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I215101

Commission Implementing Regulation (EU) No 369/2013 approving the active substance potassium phosphonates, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I550102

Commission Implementing Regulation (EU) No 373/2013 approving the active substance Candida oleophila strain O, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I542103

Commission Implementing Regulation (EU) No 375/2013 approving the active substance spiromesifen, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I517104

Commission Implementing Regulation (EU) No 378/2013 approving the active substance Paecilomyces fumosoroseus strain FE 9901, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I185105

Commission Implementing Regulation (EU) No 485/2013 amending Implementing Regulation (EU) No 540/2011, as regards the conditions of approval of the active substances clothianidin, thiamethoxam and imidacloprid, and prohibiting the use and sale of seeds treated with plant protection products containing those active substances.

I385106

Commission Implementing Regulation (EU) No 532/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance carbon dioxide.

I130107

Commission Implementing Regulation (EU) No 533/2013 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methyl-cyclopropene, chlorothalonil, chlorotoluron, cypermethrin, daminozide, forchlorfenuron, indoxacarb, thiophanate-methyl and tribenuron.

I414108

Commission Implementing Regulation (EU) No 546/2013 approving the active substance eugenol, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I382109

Commission Implementing Regulation (EU) No 568/2013 approving the active substance thymol, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I85110

Commission Implementing Regulation (EU) No 570/2013 approving the active substance geraniol, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I396111

Commission Implementing Regulation (EU) No 762/2013 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances chlorpyrifos, chlorpyrifos-methyl, mancozeb, maneb, MCPA, MCPB and metiram.

I142112

Commission Implementing Regulation (EU) No 767/2013 withdrawing the approval of the active substance bitertanol, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I99113

Commission Implementing Regulation (EU) No 781/2013 amending Implementing Regulation (EU) No 540/2011, as regards the conditions of approval of the active substance fipronil, and prohibiting the use and sale of seeds treated with plant protection products containing this active substance.

I331114

Commission Implementing Regulation (EU) No 790/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance acetic acid.

I411115

Commission Implementing Regulation (EU) No 798/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance pyrethrins.

I447116

Commission Implementing Regulation (EU) No 802/2013 approving the active substance fluopyram, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I343117

Commission Implementing Regulation (EU) No 826/2013 approving the active substance sedaxane, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I227118

Commission Implementing Regulation (EU) No 827/2013 approving the active substance Aureobasidium pullulans (strains DSM 14940 and DSM 14941), in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I143119

Commission Implementing Regulation (EU) No 828/2013 approving the active substance emamectin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I93120

Commission Implementing Regulation (EU) No 829/2013 approving the active substance Pseudomonas sp. strain DSMZ 13134, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I110121

Commission Implementing Regulation (EU) No 832/2013 approving the active substance disodium phosphonate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I446122

Commission Implementing Regulation (EU) No 833/2013 approving the active substance pyriofenone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I232123

Commission Implementing Regulation (EU) No 1031/2013 approving the active substance penflufen, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I153124

Commission Implementing Regulation (EU) No 1089/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance kieselgur (diatomaceous earth).

I149125

Commission Implementing Regulation (EU) No 1124/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance bifenox.

I205126

Commission Implementing Regulation (EU) No 1136/2013 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances clothianidin, dimoxystrobin, oxamyl and pethoxamid.

I557127

Commission Implementing Regulation (EU) No 1150/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance rape seed oil.

I453128

Commission Implementing Regulation (EU) No 1165/2013 approving the active substance orange oil, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I497129

Commission Implementing Regulation (EU) No 1166/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance dichlorprop-P.

I587130

Commission Implementing Regulation (EU) No 1175/2013 approving the active substance benalaxyl-M, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I276131

Commission Implementing Regulation (EU) No 1176/2013 approving the active substance pyroxsulam, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I113132

Commission Implementing Regulation (EU) No 1177/2013 approving the active substance spirotetramat, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I28133

Commission Implementing Regulation (EU) No 1178/2013 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance ethoprophos.

I406134

Commission Implementing Regulation (EU) No 1187/2013 approving the active substance penthiopyrad, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I395135

Commission Implementing Regulation (EU) No 1192/2013 approving the active substance tembotrione, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I144136

Commission Implementing Regulation (EU) No 1195/2013 approving the active substance sodium silver thiosulfate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I84137

Commission Implementing Regulation (EU) No 1199/2013 approving the active substance chlorantraniliprole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I181138

Commission Implementing Regulation (EU) No 85/2014 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval period of the active substance copper compounds.

I569139

Commission Implementing Regulation (EU) No 108/2014 concerning the non-approval of the active substance potassium thiocyanate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I197140

Commission Implementing Regulation (EU) No 116/2014 concerning the non-approval of the active substance potassium iodide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I104141

Commission Implementing Regulation (EU) No 140/2014 approving the active substance spinetoram, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I136142

Commission Implementing Regulation (EU) No 141/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance plant oils/clove oil.

I286143

Commission Implementing Regulation (EU) No 143/2014 approving the active substance pyridalyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I499144

Commission Implementing Regulation (EU) No 144/2014 approving the active substance valifenalate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I435145

Commission Implementing Regulation (EU) No 145/2014 approving the active substance thiencarbazone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I172146

Commission Implementing Regulation (EU) No 149/2014 approving the active substance L-ascorbic acid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I451147

Commission Implementing Regulation (EU) No 151/2014 approving the active substance S-abscisic acid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I296148

Commission Implementing Regulation (EU) No 154/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance extract from tea tree.

I97149

Commission Regulation (EU) No 186/2014 amending Regulation (EU) No 823/2012 as regards the expiry dates of the approval of the active substances ethoxysulfuron, oxadiargyl and warfarin.

I15150

Commission Implementing Regulation (EU) No 187/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance methiocarb.

I36151

Commission Implementing Regulation (EU) No 192/2014 approving the active substance F121,4-dimethylnaphthalene , in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I418152

Commission Implementing Regulation (EU) No 193/2014 approving the active substance amisulbrom, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I51153

Commission Regulation (EU) No 460/2014 amending Regulation (EU) No 823/2012 as regards the expiry date of the approval of the active substance cyfluthrin.

I189154

Commission Implementing Regulation (EU) No 462/2014 approving the basic substance Equisetum arvense L., in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I601155

Commission Implementing Regulation (EU) No 485/2014 approving the active substance Bacillus pumilus QST 2808, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Implementing Regulation (EU) No 540/2011.

I79156

Commission Implementing Regulation (EU) No 486/2014 withdrawing the approval of the active substance fenbutatin oxide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I312157

Commission Implementing Regulation (EU) No 487/2014 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances Bacillus subtilis (Cohn 1872) Strain QST 713, identical with strain AQ 713, clodinafop, metrafenone, pirimicarb, rimsulfuron, spinosad, thiamethoxam, tolclofos-methyl and triticonazole.

I251158

Commission Implementing Regulation (EU) No 496/2014 approving the active substance acequinocyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I231159

Commission Implementing Regulation (EU) No 504/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance plant oils/citronella oil.

I254160

Commission Implementing Regulation (EU) No 563/2014 approving the basic substance chitosan hydrochloride in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I37161

Commission Implementing Regulation (EU) No 571/2014 approving the active substance ipconazole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I344162

Commission Implementing Regulation (EU) No 629/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance methyl nonyl ketone.

I342163

Commission Implementing Regulation (EU) No 632/2014 approving the active substance flubendiamide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I257164

Commission Implementing Regulation (EU) No 678/2014 amending Implementing Regulation (EU) No 540/2011 as regards the extension of approval periods of the active substances clopyralid, cyprodinil, fosetyl, pyrimethanil and trinexapac.

I592165

Commission Implementing Regulation (EU) No 698/2014 amending Regulation (EC) No 2076/2002 as regards delta-endotoxin of Bacillus thuringiensis.

I175166

Commission Implementing Regulation (EU) No 700/2014 amending Implementing Regulation (EU) No 686/2012 as regards the rapporteur Member State for the active substance dimethomorph.

I510167

Commission Implementing Regulation (EU) No 878/2014 amending Implementing Regulation (EU) No 540/2011 as regards the extension of approval periods of the active substances dichlorprop-P, metaconazole and triclopyr.

I210168

Commission Implementing Regulation (EU) No 880/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance Cydia pomonella Granulovirus (CpGV).

I46169

Commission Implementing Regulation (EU) No 890/2014 approving the active substance metobromuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I554170

Commission Implementing Regulation (EU) No 891/2014 approving the active substance aminopyralid, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I168171

Commission Implementing Regulation (EU) No 916/2014 approving the basic substance sucrose, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I208172

Commission Implementing Regulation (EU) No 917/2014 approving the active substance Streptomyces lydicus strain WYEC 108 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I76173

Commission Implementing Regulation (EU) No 918/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance Straight Chain Lepidopteran Pheromones.

I228174

Commission Implementing Regulation (EU) No 921/2014 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance tebuconazole.

I605175

Commission Implementing Regulation (EU) No 922/2014 approving the active substance metaflumizone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I502176

Commission Implementing Regulation (EU) No 1316/2014 approving the active substance Bacillus amyloliquefaciens subsp. plantarum strain D747, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and allowing Member States to extend provisional authorisations granted for that active substance.

I471177

Commission Implementing Regulation (EU) No 1330/2014 approving the active substance meptyldinocap, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I481178

Commission Implementing Regulation (EU) No 1334/2014 approving the active substance gamma-cyhalotrin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and allowing Member States to extend provisional authorisations granted for that active substance.

I555179

Commission Implementing Regulation (EU) 2015/51 approving the active substance chromafenozide, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and allowing Member States to extend provisional authorisations granted for that active substance.

I461180

Commission Implementing Regulation (EU) 2015/52 amending Implementing Regulation (EU) No 686/2012 as regards the rapporteur Member State for the active substance mecoprop-P.

I157181

Commission Implementing Regulation (EU) 2015/58 amending Implementing Regulation (EU) No 540/2011 as regards the expiry date of the approval of the active substance tepraloxydim.

I565182

Commission Implementing Regulation (EU) 2015/232 amending and correcting Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance copper compounds.

I116183

Commission Implementing Regulation (EU) 2015/306 renewing the approval of the active substance Isaria fumosorosea strain Apopka 97 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I74184

Commission Implementing Regulation (EU) 2015/307 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance triclopyr.

I174185

Commission Implementing Regulation (EU) 2015/308 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance Z,Z,Z,Z-7,13,16,19-docosatetraen-1-yl isobutyrate.

I70186

Commission Implementing Regulation (EU) 2015/404 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances beflubutamid, captan, dimethoate, dimethomorph, ethoprophos, fipronil, folpet, formetanate, glufosinate, methiocarb, metribuzin, phosmet, pirimiphos-methyl and propamocarb.

I297187

Commission Implementing Regulation (EU) 2015/408 on implementing Article 80(7) of Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market and establishing a list of candidates for substitution.

I71188

Commission Implementing Regulation (EU) 2015/415 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances ethephon and fenamiphos.

I248189

Commission Implementing Regulation (EU) 2015/418 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance Z-13-hexadecen-11-yn-1-yl acetate.

I437190

Commission Implementing Regulation (EU) 2015/543 approving the active substance COS-OGA, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I515191

Commission Implementing Regulation (EU) 2015/553 approving the active substance cerevisane, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I523192

Commission Implementing Regulation (EU) 2015/707 concerning the non-approval of Rheum officinale root extract as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I316193

Commission Implementing Regulation (EU) 2015/762 approving the basic substance calcium hydroxide in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I298194

Commission Implementing Regulation (EU) 2015/1106 amending Implementing Regulations (EU) No 540/2011 and (EU) No 1037/2012 as regards the conditions of approval of the active substance isopyrazam.

I235195

Commission Implementing Regulation (EU) 2015/1107 approving the basic substance Salix spp. cortex, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I348196

Commission Implementing Regulation (EU) 2015/1108 approving the basic substance vinegar in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I370197

Commission Implementing Regulation (EU) 2015/1115 renewing the approval of the active substance pyridate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I30198

Commission Implementing Regulation (EU) 2015/1116 approving the basic substance lecithins, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I72199

Commission Implementing Regulation (EU) 2015/1154 renewing the approval of the active substance sulfosulfuron in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I391200

Commission Implementing Regulation (EU) 2015/1165 approving the active substance halauxifen-methyl, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I351201

Commission Implementing Regulation (EU) 2015/1166 renewing the approval of the active substance ferric phosphate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I233202

Commission Implementing Regulation (EU) 2015/1176 approving the active substance Pepino mosaic virus strain CH2 isolate 1906, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I52203

Commission Implementing Regulation (EU) 2015/1191 concerning the non-approval of Artemisia vulgaris L. as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I503204

Commission Implementing Regulation (EU) 2015/1192 approving the active substance terpenoid blend QRD 460, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I240205

Commission Implementing Regulation (EU) 2015/1201 renewing the approval of the active substance fenhexamid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I156206

Commission Implementing Regulation (EU) 2015/1295 approving the active substance sulfoxaflor, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I261207

Commission Implementing Regulation (EU) 2015/1392 approving the basic substance fructose in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I508208

Commission Implementing Regulation (EU) 2015/1396 correcting Implementing Regulation (EU) No 540/2011 as regards the active substance Bacillus subtilis (Cohn 1872) strain QST 713, identical with strain AQ 713.

I332209

Commission Implementing Regulation (EU) 2015/1397 renewing the approval of the active substance florasulam in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I445210

Commission Implementing Regulation (EU) 2015/1885 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2,4-D, acibenzolar-s-methyl, amitrole, bentazone, cyhalofop butyl, diquat, esfenvalerate, famoxadone, flumioxazine, DPX KE 459 (flupyrsulfuron-methyl), glyphosate, iprovalicarb, isoproturon, lambda-cyhalothrin, metalaxyl-M, metsulfuron methyl, picolinafen, prosulfuron, pymetrozine, pyraflufen-ethyl, thiabendazole, thifensulfuron-methyl and triasulfuron.

I553211

Commission Implementing Regulation (EU) 2015/2033 renewing the approval of the active substance 2,4-D in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I573212

Commission Implementing Regulation (EU) 2015/2046 concerning the non-approval of Artemisia absinthium L. as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I369213

Commission Implementing Regulation (EU) 2015/2047 renewing the approval of the active substance esfenvalerate, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I526214

Commission Implementing Regulation (EU) 2015/2069 approving the basic substance sodium hydrogen carbonate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I457215

Commission Implementing Regulation (EU) 2015/2082 concerning the non-approval of Arctium lappa L. (aerial parts) as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I221216

Commission Implementing Regulation (EU) 2015/2083 concerning the non-approval of Tanacetum vulgare L. as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I397217

Commission Implementing Regulation (EU) 2015/2084 approving the active substance flupyradifurone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I593218

Commission Implementing Regulation (EU) 2015/2085 approving the active substance mandestrobin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I292219

Commission Implementing Regulation (EU) 2015/2105 approving the active substance flumetralin, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I467220

Commission Implementing Regulation (EU) 2015/2198 approving the active substance rescalure, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I238221

Commission Implementing Regulation (EU) 2015/2233 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance haloxyfop-P.

I594222

Commission Implementing Regulation (EU) 2016/138 concerning the non-approval of the active substance 3-decen-2-one, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I350223

Commission Implementing Regulation (EU) 2016/139 renewing the approval of the active substance metsulfuron-methyl, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I237224

Commission Implementing Regulation (EU) 2016/146 renewing the approval of the active substance lambda-cyhalothrin, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I438225

Commission Implementing Regulation (EU) 2016/147 renewing the approval of the active substance iprovalicarb in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I68226

Commission Implementing Regulation (EU) 2016/177 approving the active substance benzovindiflupyr, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Implementing Regulation (EU) No 540/2011.

I323227

Commission Implementing Regulation (EU) 2016/182 renewing the approval of the active substance pyraflufen-ethyl in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I319228

Commission Implementing Regulation (EU) 2016/183 amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest.

I101229

Commission Implementing Regulation (EU) 2016/370 approving the active substance pinoxaden, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, amending the Annex to Commission Implementing Regulation (EU) No 540/2011 and allowing the Member States to extend provisional authorisations granted for that active substance.

I600230

Commission Implementing Regulation (EU) 2016/389 renewing the approval of the active substance acibenzolar-S-methyl in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I548231

Commission Implementing Regulation (EU) 2016/548 approving the basic substance diammonium phosphate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I132232

Commission Implementing Regulation (EU) 2016/549 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances bentazone, cyhalofop butyl, diquat, famoxadone, flumioxazine, DPX KE 459 (flupyrsulfuron-methyl), metalaxyl-M, picolinafen, prosulfuron, pymetrozine, thiabendazole and thifensulfuron-methyl.

I270233

Commission Implementing Regulation (EU) 2016/560 approving the basic substance whey in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I285234

Commission Implementing Regulation (EU) 2016/636 withdrawing the approval of the active substance Z,Z,Z,Z-7,13,16,19-docosatetraen-1-yl isobutyrate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council, and amending Commission Implementing Regulation (EU) No 540/2011.

I304235

Commission Implementing Regulation (EU) 2016/638 withdrawing the approval of the active substance Z-13-hexadecen-11-yn-1-yl acetate, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council, and amending Commission Implementing Regulation (EU) No 540/2011.

I536236

Commission Implementing Regulation (EU) 2016/864 concerning the non-renewal of approval of the active substance triasulfuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I56237

Commission Implementing Regulation (EU) 2016/871 concerning the non-renewal of approval of the active substance amitrole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I427238

Commission Implementing Regulation (EU) 2016/872 concerning the non-renewal of approval of the active substance isoproturon, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I498239

Commission Implementing Regulation (EU) 2016/950 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2,4-DB, beta-cyfluthrin, carfentrazone ethyl, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), cyazofamid, deltamethrin, dimethenamid-P, ethofumesate, fenamidone, flufenacet, flurtamone, foramsulfuron, fosthiazate, imazamox, iodosulfuron, iprodione, isoxaflutole, linuron, maleic hydrazide, mesotrione, oxasulfuron, pendimethalin, picoxystrobin, silthiofam and trifloxystrobin.

I146240

Commission Implementing Regulation (EU) 2016/951 approving the low-risk active substance Trichoderma atroviride strain SC1, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I494241

Commission Implementing Regulation (EU) 2016/952 approving the low-risk active substance Saccharomyces cerevisiae strain LAS02 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I598242

Commission Implementing Regulation (EU) 2016/1056 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval period of the active substance glyphosate.

I516243

Commission Implementing Regulation (EU) 2016/1313 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance glyphosate.

I578244

Commission Implementing Regulation (EU) 2016/1414 approving the active substance cyantraniliprole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I87245

Commission Implementing Regulation (EU) 2016/1423 renewing approval of the active substance picolinafen in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I379246

Commission Implementing Regulation (EU) 2016/1424 renewing the approval of the active substance thifensulfuron-methyl in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I575247

Commission Implementing Regulation (EU) 2016/1425 approving the active substance isofetamid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I353248

Commission Implementing Regulation (EU) 2016/1426 renewing the approval of the active substance ethofumesate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I176249

Commission Implementing Regulation (EU) 2016/1429 approving the active substance Bacillus amyloliquefaciens strain MBI 600, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I514250

Commission Implementing Regulation (EU) 2016/1826 concerning the non-approval of the active substance tricyclazole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I224251

Commission Implementing Regulation (EU) 2016/1978 approving the basic substance sunflower oil in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I198252

Commission Implementing Regulation (EU) 2016/2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances acetamiprid, benzoic acid, flazasulfuron, mecoprop-P, mepanipyrim, mesosulfuron, propineb, propoxycarbazon, propyzamide, propiconazole, Pseudomonas chlororaphis Strain: MA 342, pyraclostrobin, quinoxyfen, thiacloprid, thiram, ziram, zoxamide.

I287253

Commission Implementing Regulation (EU) 2016/2035 amending Implementing Regulation (EU) No 540/2011 as regards the approval periods of the active substances fipronil and maneb.

I530254

Commission Implementing Regulation (EU) 2017/157 renewing the approval of the active substance thiabendazole in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I253255

Commission Implementing Regulation (EU) 2017/195 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of several active substances listed in Part B of the Annex to Implementing Regulation (EU) No 686/2012 (AIR IV renewal programme).

I402256

Commission Implementing Regulation (EU) 2017/239 approving the active substance oxathiapiprolin in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I463257

Commission Implementing Regulation (EU) 2017/240 concerning the non-approval of Satureja montana L. essential oil as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I373258

Commission Implementing Regulation (EU) 2017/241 concerning the non-approval of Origanum vulgare L. essential oil as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I102259

Commission Implementing Regulation (EU) 2017/243 amending Implementing Regulation (EU) No 686/2012 as regards the co-rapporteur Member State for the active substance metaldehyde.

I357260

Commission Implementing Regulation (EU) 2017/244 concerning the non-renewal of approval of the active substance linuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I275261

Commission Implementing Regulation (EU) 2017/270 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance sulfuryl fluoride.

I182262

Commission Implementing Regulation (EU) 2017/357 concerning the non-approval of the active substance cyclaniliprole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I32263

Commission Implementing Regulation (EU) 2017/358 confirming the conditions of approval of the active substance acrinathrin, as set out in Implementing Regulation (EU) No 540/2011.

I11264

Commission Implementing Regulation (EU) 2017/359 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance oxyfluorfen.

I364265

Commission Implementing Regulation (EU) 2017/360 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance buprofezin.

I2266

Commission Implementing Regulation (EU) 2017/375 renewing the approval of the active substance prosulfuron, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I367267

Commission Implementing Regulation (EU) 2017/377 concerning the non-approval of the active substance Pseudozyma flocculosa strain ATCC 64874 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I294268

Commission Implementing Regulation (EU) 2017/406 approving the low-risk active substance Mild Pepino Mosaic Virus isolate VX1, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I219269

Commission Implementing Regulation (EU) 2017/407 renewing the approval of the active substance iodosulfuron in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I525270

Commission Implementing Regulation (EU) 2017/408 approving the low-risk active substance Mild Pepino Mosaic Virus isolate VC1, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I612271

Commission Implementing Regulation (EU) 2017/409 approving the basic substance hydrogen peroxide in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I507272

Commission Implementing Regulation (EU) 2017/419 approving the basic substance Urtica spp. in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I366273

Commission Implementing Regulation (EU) 2017/428 approving the basic substance clayed charcoal in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I394274

Commission Implementing Regulation (EU) 2017/438 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance abamectin.

I371275

Commission Implementing Regulation (EU) 2017/555 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of several active substances listed in Part B of the Annex to Implementing Regulation (EU) No 686/2012 (AIR IV renewal programme).

I8276

Commission Implementing Regulation (EU) 2017/725 renewing the approval of the active substance mesotrione in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I41277

Commission Implementing Regulation (EU) 2017/753 renewing the approval of the active substance cyhalofop-butyl in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I218278

Commission Implementing Regulation (EU) 2017/755 renewing the approval of the active substance mesosulfuron in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I333279

Commission Implementing Regulation (EU) 2017/781 withdrawing the approval of the active substance methyl nonyl ketone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I596280

Commission Implementing Regulation (EU) 2017/805 renewing the approval of the active substance flazasulfuron in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I178281

Commission Implementing Regulation (EU) 2017/806 approving the low-risk active substance Bacillus amyloliquefaciens strain FZB24, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I89282

Commission Implementing Regulation (EU) 2017/831 approving the active substance Beauveria bassiana strain 147, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I307283

Commission Implementing Regulation (EU) 2017/840 concerning the non-approval of the active substance orthosulfamuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I117284

Commission Implementing Regulation (EU) 2017/841 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances alpha-cypermethrin, Ampelomyces quisqualis strain: aq 10, benalaxyl, bentazone, bifenazate, bromoxynil, carfentrazone ethyl, chlorpropham, cyazofamid, desmedipham, diquat, DPX KE 459 (flupyrsulfuron-methyl), etoxazole, famoxadone, fenamidone, flumioxazine, foramsulfuron, Gliocladium catenulatum strain: j1446, imazamox, imazosulfuron, isoxaflutole, laminarin, metalaxyl-m, methoxyfenozide, milbemectin, oxasulfuron, pendimethalin, phenmedipham, pymetrozine, s-metolachlor, and trifloxystrobin.

I450285

Commission Implement Regulation (EU) 2017/842 renewing the approval of the low-risk active substance Coniothyrium minitans strain CON/M/91-08 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I137286

Commission Implementing Regulation (EU) 2017/843 approving the active substance Beauveria bassiana strain NPP111B005, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I27287

Commission Implementing Regulation (EU) 2017/855 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance diflubenzuron.

I179288

Commission Implementing Regulation (EU) 2017/856 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance fluroxypyr.

I256289

Commission Implementing Regulation (EU) 2017/1113 renewing the approval of the active substance benzoic acid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I570290

Commission Implementing Regulation (EU) 2017/1114 renewing the approval of the active substance pendimethalin, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I460291

Commission Implementing Regulation (EU) 2017/1115 renewing the approval of the active substance propoxycarbazone in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I390292

Commission Implementing Regulation (EU) 2017/1125 withdrawing the approval of the active substance repellents by smell of animal or plant origin/tall oil pitch, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I207293

Commission Implementing Regulation (EU) 2017/1186 withdrawing the approval of the active substance repellents by smell of animal or plant origin/tall oil crude, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I20294

Commission Implementing Regulation (EU) 2017/1455 concerning the non-renewal of approval of the active substance picoxystrobin, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I69295

Commission Implementing Regulation (EU) 2017/1491 renewing the approval of the active substance 2,4-DB in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I234296

Commission Implementing Regulation (EU) 2017/1496 concerning the non-renewal of approval of the active substance DPX KE 459 (flupyrsulfuron-methyl), in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I216297

Commission Implementing Regulation (EU) 2017/1506 renewing the approval of the active substance maleic hydrazide in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I124298

Commission Implementing Regulation (EU) 2017/1511 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, cypermethrin, daminozide, deltamethrin, dimethenamid-p, flufenacet, flurtamone, forchlorfenuron, fosthiazate, indoxacarb, iprodione, MCPA, MCPB, silthiofam, thiophanate-methyl and tribenuron.

I484299

Commission Implementing Regulation (EU) 2017/1526 concerning the non-approval of the active substance beta-cypermethrin in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I49300

Commission Implementing Regulation (EU) 2017/1527 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances cyflufenamid, fluopicolide, heptamaloxyloglucan and malathion.

I478301

Commission Implementing Regulation (EU) 2017/1529 approving the basic substance sodium chloride in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I21302

Commission Implementing Regulation (EU) 2017/1530 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval period of the active substance quizalofop-p-tefuryl.

I595303

Commission Implementing Regulation (EU) 2017/1531 renewing the approval of the active substance imazamox, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I103304

Commission Implementing Regulation (EU) 2017/2057 concerning the non-approval of Achillea millefolium L. as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I469305

Commission Implementing Regulation (EU) 2017/2065 confirming the conditions of approval of the active substance 8-hydroxyquinoline, as set out in Implementing Regulation (EU) No 540/2011 and modifying Implementing Regulation (EU) 2015/408 as regards the inclusion of the active substance 8-hydroxyquinoline in the list of candidates for substitution.

I206306

Commission Implementing Regulation (EU) 2017/2066 concerning the approval of mustard seeds powder as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I108307

Commission Implementing Regulation (EU) 2017/2067 concerning the non-approval of paprika extract (capsanthin, capsorubin E 160 c) as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I199308

Commission Implementing Regulation (EU) 2017/2068 concerning the non-approval of potassium sorbate as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I546309

Commission Implementing Regulation (EU) 2017/2069 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances flonicamid (IKI-220), metalaxyl, penoxsulam and proquinazid.

I300310

Commission Implementing Regulation (EU) 2017/2090 concerning the approval of beer as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I329311

Commission Implementing Regulation (EU) 2017/2091 concerning the non-renewal of approval of the active substance iprodione, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I18312

Commission Implementing Regulation (EU) 2017/2324 renewing the approval of the active substance glyphosate in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I222313

Commission Implementing Regulation (EU) 2018/84 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances chlorpyrifos, chlorpyrifos-methyl, clothianidin, copper compounds, dimoxystrobin, mancozeb, mecoprop-p, metiram, oxamyl, pethoxamid, propiconazole, propineb, propyzamide, pyraclostrobin and zoxamide.

I90314

Commission Implementing Regulation (EU) 2018/112 renewing the approval of the low-risk active substance laminarin in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I48315

Commission Implementing Regulation (EU) 2018/113 renewing the approval of the active substance acetamiprid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I501316

Commission Implementing Regulation (EU) 2018/155 amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of active substances.

I509317

Commission Implementing Regulation (EU) 2018/184 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances FEN 560 (also called fenugreek or fenugreek seed powder) and sulfuryl fluoride.

I493318

Commission Implementing Regulation (EU) 2018/185 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance penflufen.

I386319

Commission Implementing Regulation (EU) 2018/291 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance bifenthrin.

I543320

Commission Implementing Regulation (EU) 2018/309 concerning the non-renewal of approval of the active substance propineb, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I585321

Commission Implementing Regulation (EU) 2018/524 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances Bacillus subtilis (Cohn 1872) Strain QST 713, identical with strain AQ 713, clodinafop, clopyralid, cyprodinil, dichlorprop-P, fosetyl, mepanipyrim, metconazole, metrafenone, pirimicarb, Pseudomonas chlororaphis strain: MA 342, pyrimethanil, quinoxyfen, rimsulfuron, spinosad, thiacloprid, thiamethoxam, thiram, tolclofos-methyl, triclopyr, trinexapac, triticonazole and ziram.

I295322

Commission Implementing Regulation (EU) 2018/679 renewing the approval of the active substance forchlorfenuron in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I322323

Commission Implementing Regulation (EU) 2018/690 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance fenazaquin.

I361324

Commission Implementing Regulation (EU) 2018/691 approving the basic substance Talc E553B in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I393325

Commission Implementing Regulation (EU) 2018/692 renewing the approval of the active substance zoxamide in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I398326

Commission Implementing Regulation (EU) 2018/710 renewing the approval of the active substance silthiofam in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I489327

Commission Implementing Regulation (EU) 2018/755 renewing the approval of the active substance propyzamide, as a candidate for substitution, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I64328

Commission Implementing Regulation (EU) 2018/783 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance imidacloprid.

I188329

Commission Implementing Regulation (EU) 2018/784 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance clothianidin.

I440330

Commission Implementing Regulation (EU) 2018/785 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance thiamethoxam.

I107331

Commission Implementing Regulation (EU) 2018/917 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances alpha-cypermethrin, beflubutamid, benalaxyl, benthiavalicarb, bifenazate, boscalid, bromoxynil, captan, carvone, chlorpropham, cyazofamid, desmedipham, dimethoate, dimethomorph, diquat, ethephon, ethoprophos, etoxazole, famoxadone, fenamidone, fenamiphos, flumioxazine, fluoxastrobin, folpet, foramsulfuron, formetanate, Gliocladium catenulatum strain: J1446, isoxaflutole, metalaxyl-m, methiocarb, methoxyfenozide, metribuzin, milbemectin, oxasulfuron, Paecilomyces lilacinus strain 251, phenmedipham, phosmet, pirimiphos-methyl, propamocarb, prothioconazole, pymetrozine and s-metolachlor.

I590332

Commission Implementing Regulation (EU) 2018/1019 concerning the non-renewal of approval of the active substance oxasulfuron, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I180333

Commission Implementing Regulation (EU) 2018/1043 concerning the non-renewal of approval of the active substance fenamidone, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I23334

Commission Implementing Regulation (EU) 2018/1060 renewing the approval of the active substance trifloxystrobin in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I167335

Commission Implementing Regulation (EU) 2018/1061 renewing the approval of the active substance carfentrazone-ethyl in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I133336

Commission Implementing Regulation (EU) 2018/1075 renewing the approval of the active substance Ampelomyces quisqualis strain AQ10, as a low-risk active substance, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I170337

Commission Implementing Regulation (EU) 2018/1260 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances pyridaben, quinmerac and zinc phosphide.

I57338

Commission Implementing Regulation (EU) 2018/1262 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, clomazone, cypermethrin, daminozide, deltamethrin, dimethenamid-p, diuron, fludioxonil, flufenacet, flurtamone, fosthiazate, indoxacarb, MCPA, MCPB, prosulfocarb, thiophanate-methyl and tribenuron.

I545339

Commission Implementing Regulation (EU) 2018/1264 renewing the approval of the active substance pethoxamid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I607340

Commission Implementing Regulation (EU) 2018/1265 approving the active substance fenpicoxamid in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I422341

Commission Implementing Regulation (EU) 2018/1266 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-decanol, 6-benzyladenine, aluminium sulfate, azadirachtin, bupirimate, carboxin, clethodim, cycloxydim, dazomet, diclofop, dithianon, dodine, fenazaquin, fluometuron, flutriafol, hexythiazox, hymexazol, indolylbutyric acid, isoxaben, lime sulphur, metaldehyde, paclobutrazol, pencycuron, sintofen, tau-fluvalinate and tebufenozide.

I121342

Commission Implementing Regulation (EU) 2018/1278 approving the low-risk active substance Pasteuria nishizawae Pn1 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I281343

Commission Implementing Regulation (EU) 2018/1294 concerning the non-approval of Landes pine tar as a basic substance in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market.

I249344

Commission Implementing Regulation (EU) 2018/1295 approving the basic substance Onion oil in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011.

I479345

Commission Implementing Regulation (EU) 2018/1495 amending Implementing Regulation (EU) No 540/2011 as regards the conditions of approval of the active substance malathion.

I431346

Commission Implementing Regulation (EU) 2018/1500 concerning the non-renewal of approval of the active substance thiram, and prohibiting the use and sale of seeds treated with plant protection products containing thiram, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I81347

Commission Implementing Regulation (EU) 2018/1501 concerning the non-renewal of approval of the active substance pymetrozine, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I470348

Commission Implementing Regulation (EU) 2018/1532 concerning the non-renewal of approval of the active substance diquat, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

I283349

Commission Implementing Regulation (EU) 2018/1796 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances amidosulfuron, bifenox, chlorpyrifos, chlorpyrifos-methyl, clofentezine, dicamba, difenoconazole, diflubenzuron, diflufenican, dimoxystrobin, fenoxaprop-p, fenpropidin, lenacil, mancozeb, mecoprop-p, metiram, nicosulfuron, oxamyl, picloram, pyraclostrobin, pyriproxyfen and tritosulfuron.

I24350

Commission Implementing Regulation (EU) 2018/1865 concerning the non-renewal of approval of the active substance propiconazole, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending Commission Implementing Regulation (EU) No 540/2011.

PART 2Decisions

I429351

Commission Decision No 94/643/EC concerning the withdrawal of authorizations for plant protection products containing cyhalothrin as active substance.

I559352

Commission Decision No 95/276/EC concerning the withdrawal of authorizations for plant protection products containing ferbam or azinphos-ethyl as active substances.

I115353

Commission Decision No 96/266/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of kresoxim methyl in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I129354

Commission Decision No 96/341/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of flurtamone in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I127355

Commission Decision No 96/457/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of quinoxyfen in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I568356

Commission Decision No 96/520/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of prohexadione calcium in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I400357

Commission Decision No 96/521/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of chlorfenapyr in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I55358

Commission Decision No 96/522/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of spiroxamine in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I35359

Commission Decision No 96/523/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of azoxystrobin in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I203360

Commission Decision No 96/524/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of isoxaflutole in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I334361

Commission Decision No 96/586/EC concerning the withdrawal of authorizations for plant protection products containing propham as an active substance.

I152362

Commission Decision No 97/137/EC recognizing in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of prosulfuron and cyclanilide in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I346363

Commission Decision No 97/164/EC recognizing in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of flupyrsulfuron-methyl, azimsulfuron and paecilomyces fumosoroseus in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I340364

Commission Decision No 97/248/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of pseudomonas chlororaphis in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I365365

Commission Decision No 97/362/EC recognizing in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of carfentrazone-ethyl, fosthiazate and fluthiamide in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I78366

Commission Decision No 97/591/EC recognizing in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of mefenoxam (CGA 329 351), ethoxysulfuron, famoxadone and ampelomyces quisqualis in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I255367

Commission Decision No 97/631/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of flumioxazine in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I315368

Commission Decision No 97/865/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of CGA 245 704, flazasulfuron, Spodoptera exigua nuclear polyhedrosis virus, imazosulfuron, pymetrozine and sulfosulfuron in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I403369

Commission Decision No 98/242/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of cyhalofop-butyl, pyraflufen-ethyl and azafenidin in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I310370

Commission Decision No 98/269/EC concerning the withdrawal of authorisations for plant protection products containing dinoterb as an active substance.

I120371

Commission Decision No 98/270/EC concerning the withdrawal of authorisations for plant protection products containing fenvalerate as an active substance.

I263372

Commission Decision No 98/398/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of BAS 615H, KBR 2738 (fenhexamid), oxadiargyl and DPX-KN128 (indoxacarb) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I449373

Commission Decision No 98/512/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of BAS 620H (tepraloxydim), S-metolachlor and SZX 0722 (iprovalicarb) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I308374

Commission Decision No 98/676/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of KIF 3535 (mepanipyrim), imazamox (AC 299263), DE 570 (florasulam), fluazolat (JV 485), Coniothyrium minitans and benzoic acid in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I468375

Commission Decision No 1999/43/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of CGA 279 202 (trifloxystrobin), clefoxydim (BAS 625H), etoxazol and ferric phosphate in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I7376

Commission Decision No 1999/164/EC concerning the non-inclusion of DNOC of active substance in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I314377

Commission Decision No 1999/237/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of CGA 277 476 (oxasulfuron) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I92378

Commission Decision No 1999/392/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of ZA 1296 (mesotrione), Iodosulfuron-methyl-sodium (AEF 115008) Silthiopham (MON 65500) and Gliocladium catenulatum in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I96379

Commission Decision No 1999/555/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of BAS 656H (dimethenamid-p AC 900001(picolinafen), ZA 1963 (picoxystrobin) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I430380

Commission Decision No 1999/610/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of L 91105D (carvone) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I195381

Commission Decision No 2000/166/EC extending the possible time period for provisional authorisations of the new active substance quinoxyfen.

I158382

Commission Decision No 2000/180/EC extending the possible time period for provisional authorisations of the new active substance Pseudomonas chlororaphis.

I610383

Commission Decision No 2000/181/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of thiacloprid, forchlorfenuron, thiamethoxam in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I442384

Commission Decision No 2000/210/EC recognising in principle the completeness of the dossier submitted for detailed examination with a view to the possible inclusion of spinosad in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I588385

Commission Decision No 2000/233/EC concerning the non-inclusion of pyrazophos in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I558386

Commission Decision No 2000/234/EC concerning the non-inclusion of monolinuron in Annex I to Council Directive 91/414/EC and the withdrawal of authorisations for plant protection products containing this active substance.

I561387

Commission Decision No 2000/251/EC recognising in principle the completeness of the dossier submitted for detailed examination with a view to the possible inclusion of RPA407213 (fenamidone) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I487388

Commission Decision No 2000/358/EC extending the possible time period for provisional authorisations of the new active substances flupyrsulfuron methyl, carfentrazone ethyl, prosulfuron, flurtamone, isoxaflutole.

I421389

Commission Decision No 2000/390/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of EXP60707B (acetamiprid) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I485390

Commission Decision No 2000/412/EC recognising in principle the completeness of the dossier submitted for detailed examination with a view to the possible inclusion of IKF 916 (cyazofamid) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I384391

Commission Decision No 2000/463/EC recognising in principle the completeness of the dossier submitted for detailed examination F55with a view to the possible inclusion of MKH 65 61 (propoxycarbazone-sodium) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I190392

Commission Decision No 2000/540/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of RH-7281 (zoxamide), B-41; E-187 (milbemectin), BAS500F (pyraclostrobin) and AEF130360 (foramsulfuron) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I252393

Commission Decision No 2000/626/EC concerning the non-inclusion of chlozolinate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I191394

Commission Decision No 2000/725/EC concerning the non-inclusion of tecnazene in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I269395

Commission Decision No 2000/784/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of UBH 820;UR 50601 (beflubutamid) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I541396

Commission Decision No 2000/801/EC concerning the non-inclusion of lindane in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I417397

Commission Decision No 2000/816/EC concerning the non-inclusion of quintozene in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I567398

Commission Decision No 2000/817/EC concerning the non-inclusion of permethrin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I213399

Commission Decision No 2001/6/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of QRD 133 WP (Bacillus subtilis strain QST 713) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I106400

Commission Decision No 2001/134/EC concerning the decision on the possible inclusion of certain active substances into Annex I to Council Directive 91/414/EEC.

I360401

Commission Decision No 2001/231/EC making it possible for Member States to extend provisional authorisations granted for the new active substances IKI 1145; TO 1145 (fosthiazate), CGA 329351 (metalaxyl-m), MON 37500 (sulfosulfuron) and Spodoptera exigua nuclear polyhedrosis virus.

I320402

Commission Decision No 2001/245/EC concerning the non-inclusion of zineb in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I217403

Commission Decision No 2001/287/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of mesosulfuron methyl in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I488404

Commission Decision No 2001/315/EC making it possible for Member States to extend provisional authorisations granted for the new active substances flupyrsulfuron-methyl, carfentrazone-ethyl, famoxadone, prosulfuron, isoxaflutole, flurtamone, ethoxysulfuron, paecilomyces fumosoroseus, and cyclanilide.

I475405

Commission Decision No 2001/385/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of RH 2485 (methoxyfenozide) in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I88406

Commission Decision No 2001/520/EC concerning the non-inclusion of parathion in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I289407

Commission Decision No 2001/529/EC making it possible for Member States to extend provisional authorisations granted for the new active substances benzoic acid and BAS 615H (cinidon-ethyl).

I47408

Commission Decision No 2001/626/EC recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of Pethoxamide in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I262409

Commission Decision No 2001/679/EC concerning the decision on the possible inclusion of certain active substances into Annex I to Directive 91/414/EEC.

I415410

Commission Decision No 2001/697/EC concerning the non-inclusion of chlorfenapyr in Annex I to Council Directive 91/414/EEC.

I376411

Commission Decision No 2001/810/EC concerning the decision on the possible inclusion of certain active substances into Annex I to Directive 91/414/EEC.

I83412

Commission Decision No 2001/861/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Laminarin and Novaluron in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I576413

Commission Decision No 2002/133/EC making it possible for Member States to extend provisional authorisations granted for the new active substances carfentrazone-ethyl, cinidon-ethyl, cyhalofop-butyl, ethoxysulfuron, famoxadone, flazasulfuron, flufenacet, flumioxazine, flurtamone, fosthiazate, isoxaflutole, metalaxyl-M, prosulfuron, Pseudomonas chlororaphis, quinoxyfen, Spodoptera exigua nuclear polyhedrosis virus and sulfosulfuron.

I105414

Commission Decision No 2002/268/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of nicobifen, tritosulfuron and bifenazate in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I128415

Commission Decision No 2002/305/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of clothianidin and Pseudozyma flocculosa in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I506416

Commission Decision No 2002/311/EC repealing Decision 1999/462/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of alanycarbe in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I19417

Commission Decision No 2002/478/EC concerning the non-inclusion of fentin acetate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I560418

Commission Decision No 2002/479/EC concerning the non-inclusion of fentin hydroxide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I14419

Commission Decision No 2002/593/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Spirodiclofen and Dimoxystrobin in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I401420

Commission Decision No 2002/658/EC allowing Member States to extend provisional authorisations granted for the new active substances benzoic acid, carvone, mepanipyrim, oxadiargyl and trifloxystrobin.

I534421

Commission Decision No 2002/748/EC amending Decision 98/676/EC as regards fluazolat.

I556422

Commission Decision No 2002/928/EC concerning the non-inclusion of benomyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I413423

Commission Decision No 2002/949/EC concerning the non-inclusion of azafenidin in Annex I to Council Directive 91/414/EEC.

I265424

Commission Decision No 2003/35/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of benalaxyl-M, benthiavalicarb, 1-methylcyclopropene, prothioconazole and fluoxastrobin in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I551425

Commission Decision No 2003/105/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of spiromesifen and metrafenone in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I91426

Commission Decision No 2003/166/EC concerning the non-inclusion of parathion-methyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I582427

Commission Decision No 2003/199/EC concerning the non-inclusion of aldicarb in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I591428

Commission Decision No 2003/219/EC concerning the non-inclusion of acephate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I405429

Commission Decision No 2003/305/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of sulphuryl fluoride, bispyribac sodium and paecilomyces lilacinus in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I187430

Commission Decision No 2003/308/EC concerning the non-inclusion of metalaxyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I34431

Commission Decision No 2003/370/EC allowing Member States to extend provisional authorisations granted for the new active substances iodosulfuron-methyl-sodium, indoxacarb, S-metolachlor, Spodoptera exigua nuclear polyhedrosis virus, tepraloxydim and dimethenamid-P.

I477432

Commission Decision No 2003/636/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of potassium phosphite, acequinocyl and cyflufenamid in Annex 1 to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I464433

Commission Decision No 2003/850/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of BAS 670H and silver thiosulphate in Annex I to Council Directive 91/414/EEC concerning the placing of plant protection products on the market.

I544434

Commission Decision No 2003/896/EC allowing Member States to extend provisional authorisations granted for the new active substances thiacloprid, thiametoxam, quinoxyfen, flazasulfuron, Spodoptera exigua nuclear polyhedrosis virus, spinosad, Giocladium catenulatum, Pseudomonas chlororaphis and indoxacarb.

I112435

Commission Decision No 2004/129/EC concerning the non-inclusion of certain active substances in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I434436

Commission Decision No 2004/131/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of FEN 560 and penoxsulam in Annex I to Council Directive 91/414/EEC.

I98437

Commission Decision No 2004/140/EC concerning the non-inclusion of fenthion in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I577438

Commission Decision No 2004/141/EC concerning the non-inclusion of amitraz in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I31439

Commission Decision No 2004/247/EC concerning the non-inclusion of simazine in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I347440

Commission Decision No 2004/248/EC concerning the non-inclusion of atrazine in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I491441

Commission Decision No 2004/390/EC allowing Member States to extend provisional authorisations granted for the new active substance acetamiprid.

I54442

Commission Decision No 2004/400/EC allowing Member States to extend provisional authorisations granted for the new active substance profoxydim.

I299443

Commission Decision No 2004/401/EC concerning the non-inclusion of mefluidide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this substance.

I131444

Commission Decision No 2004/627/EC allowing Member States to extend provisional authorisations granted for the new active substances etoxazole and carvone.

I38445

Commission Decision No 2004/686/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of proquinazid, IKI-220 (flonicamid) and gamma-cyhalothrin in Annex I to Council Directive 91/414/EEC.

I114446

Commission Decision No 2005/303/EC concerning the non-inclusion of cresylic acid, dichlorophen, imazamethabenz, kasugamycin and polyoxin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I330447

Commission Decision No 2005/459/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of pinoxaden in Annex I to Council Directive 91/414/EEC.

I247448

Commission Decision No 2005/487/EC concerning the non-inclusion of triazamate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I211449

Commission Decision No 2005/743/EC allowing Member States to extend provisional authorisations granted for the new active substances boscalid, indoxacarb, spinosad and Spodoptera exigua nuclear polyhedrosis virus.

I519450

Commission Decision No 2005/751/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of ascorbic acid, potassium iodide and potassium thiocyanate in Annex I to Council Directive 91/414/EEC.

I474451

Commission Decision No 2005/778/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of aminopyralid and fluopicolide in Annex I to Council Directive 91/414/EEC.

I196452

Commission Decision No 2005/788/EC concerning the non-inclusion of naled in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I50453

Commission Decision No 2005/864/EC concerning the non-inclusion of endosulfan in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I77454

Commission Decision No 2006/131/EC allowing Member States to extend provisional authorisations granted for the new active substance thiamethoxam.

I602455

Commission Decision No 2006/302/EC concerning the non-inclusion of methabenzthiazuron in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I328456

Commission Decision No 2006/409/EC allowing Member States to extend provisional authorisations granted for the new active substance profoxydim.

I126457

Commission Decision No 2006/517/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of metaflumizone in Annex I to Council Directive 91/414/EEC.

I194458

Commission Decision No 2006/584/EC allowing Member States to extend provisional authorisations granted for the new active substance beflubutamid.

I123459

Commission Decision No 2006/586/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of chromafenozide, halosulfuron, tembotrione, valiphenal and Zucchini yellow mosaic virus — weak strain in Annex I to Council Directive 91/414/EEC.

I388460

Commission Decision No 2006/589/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of aviglycine HCl, mandipropamid and meptyldinocap in Annex I to Council Directive 91/414/EEC.

I109461

Commission Decision No 2006/797/EC concerning the non-inclusion of ammonium sulphamate, hexaconazole, sodium tetrathiocarbonate and 8-hydroxyquinoline in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these active substances.

I204462

Commission Decision No 2006/806/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of orthosulfamuron in Annex I to Council Directive 91/414/EEC.

I226463

Commission Decision No 2006/927/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of flubendiamide in Annex I of Council Directive 91/414/EEC.

I65464

Commission Decision No 2006/966/EC concerning the non-inclusion of alachlor in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing this active substance.

I311465

Commission Decision No 2006/1009/EC concerning the non-inclusion of dimethenamid in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I60466

Commission Decision No 2006/1010/EC concerning the non-inclusion of phosalone in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I260467

Commission Decision No 2007/67/EC allowing Member States to extend provisional authorisations granted for the new active substance tritosulfuron.

I274468

Commission Decision No 2007/277/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of pyroxsulam in Annex I to Council Directive 91/414/EEC.

I148469

Commission Decision No 2007/322/EC laying down protective measures concerning uses of plant protection products containing tolylfluanid leading to the contamination of drinking water.

I139470

Commission Decision No 2007/355/EC concerning the non-inclusion of carbaryl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I186471

Commission Decision No 2007/356/EC concerning the non-inclusion of trichlorfon in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I524472

Commission Decision No 2007/366/EC concerning the non-inclusion of thiodicarb in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I433473

Commission Decision No 2007/379/EC concerning the non-inclusion of fenitrothion in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I459474

Commission Decision No 2007/380/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Candida oleophila strain O in Annex I to Council Directive 91/414/EEC.

I42475

Commission Decision No 2007/387/EC concerning the non-inclusion of dichlorvos in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I63476

Commission Decision No 2007/389/EC concerning the non-inclusion of malathion in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I408477

Commission Decision No 2007/392/EC concerning the non-inclusion of oxydemeton-methyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I583478

Commission Decision No 2007/393/EC concerning the non-inclusion of diazinon in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I374479

Commission Decision No 2007/396/EC repealing Decision 2004/409/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of ethaboxam in Annex I to Council Directive 91/414/EEC.

I571480

Commission Decision No 2007/415/EC concerning the non-inclusion of carbosulfan in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I317481

Commission Decision No 2007/416/EC concerning the non-inclusion of carbofuran in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I574482

Commission Decision No 2007/417/EC concerning the non-inclusion of diuron in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I586483

Commission Decision No 2007/428/EC concerning the non-inclusion of cadusafos in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I399484

Commission Decision No 2007/437/EC concerning the non-inclusion of haloxyfop-R in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I9485

Commission Decision No 2007/442/EC concerning the non-inclusion of certain active substances in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I305486

Commission Decision No 2007/553/EC concerning the non-inclusion of monocarbamide dihydrogensulphate and dimethipin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these active substances.

I528487

Commission Decision No 2007/560/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of chlorantraniliprole, heptamaloxyglucan, spirotetramat and Helicoverpa armigera nucleopolyhedrovirus in Annex I to Council Directive 91/414/EEC.

I482488

Commission Decision No 2007/615/EC concerning the non-inclusion of benufuracarb in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I80489

Commission Decision No 2007/619/EC concerning the non-inclusion of 1,3-dichloropropene in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I183490

Commission Decision No 2007/628/EC concerning the non-inclusion of methomyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I302491

Commission Decision No 2007/629/EC concerning the non-inclusion of trifluralin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I540492

Commission Decision No 2007/669/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Adoxophyes orana granulovirus, amisulbrom, emamectin, pyridalil and Spodoptera littoralis nucleopolyhedrovirus in Annex I to Council Directive 91/414/EEC.

I448493

Commission Decision No 2007/758/EC allowing Member States to extend provisional authorisations granted for the new active substance boscalid.

I267494

Commission Decision No 2008/20/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of ipconazole and maltodextrin in Annex I to Council Directive 91/414/EEC.

I597495

Commission Decision No 2008/278/EC amending Decision 2006/589/EC as regards aviglycine HCI.

I423496

Commission Decision No 2008/296/EC concerning the non-inclusion of azocyclotin, cyhexatin and thidiazuron in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing those active substances.

I277497

Commission Decision No 2008/317/EC concerning the non-inclusion of rotenone, extract from equisetum and chinin-hydrochlorid in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I492498

Commission Decision No 2008/353/EC allowing Member States to extend provisional authorisations granted for the new active substances cyflufenamid, FEN 560 and flonicamid.

I58499

Commission Decision No 2008/564/EC allowing Member States to extend provisional authorisations granted for the new active substance profoxydim.

I387500

Commission Decision No 2008/565/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Paecilomyces fumosoroseus strain Fe 9901 and Trichoderma atroviride strain I-1237 in Annex I to Council Directive 91/414/EEC.

I511501

Commission Decision No 2008/566/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of phosphane and thiencarbazone in Annex I to Council Directive 91/414/EEC.

I202502

Commission Decision No 2008/599/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of Pseudomonas sp. strain DMZ 13134 in Annex I to Council Directive 91/414/EEC.

I389503

Commission Decision No 2008/656/EC on the admissibility of the notifications concerning the renewal of the inclusion in Annex I to Council Directive 91/414/EEC of the active substances azimsulfuron, azoxystrobin, fluroxypyr, imazalil, kresoxim-methyl, prohexadion-calcium and spiroxamin, and establishing the list of the notifiers concerned.

I375504

Commission Decision No 2008/724/EC allowing Member States to extend provisional authorisations granted for the new active substances fluopicolide and pinoxaden.

I327505

Commission Decision No 2008/740/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of spinetoram in Annex I to Council Directive 91/414/EEC.

I549506

Commission Decision No 2008/742/EC concerning the non-inclusion of propachlor in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I358507

Commission Decision No 2008/743/EC concerning the non-inclusion of diniconazole-M in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I441508

Commission Decision No 2008/745/EC concerning the non-inclusion of cyanamide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I518509

Commission Decision No 2008/748/EC concerning the non-inclusion of triflumizole in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I490510

Commission Decision No 2008/764/EC concerning the non-inclusion of dicofol in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I606511

Commission Decision No 2008/768/EC concerning the non-inclusion of Beauveria brongniartii and potassium permanganate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I271512

Commission Decision No 2008/770/EC concerning the non-inclusion of tricyclazole in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I378513

Commission Decision No 2008/771/EC concerning the non-inclusion of buprofezin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I608514

Commission Decision No 2008/819/EC concerning the non-inclusion of butralin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I264515

Commission Decision No 2008/832/EC concerning the non-inclusion of bromuconazole in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I483516

Commission Decision No 2008/865/EC concerning the non-inclusion of chlorate in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I95517

Commission Decision No 2008/902/EC concerning the non-inclusion of napropamide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I380518

Commission Decision No 2008/934/EC concerning the non-inclusion of certain active substances in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I86519

Commission Decision No 2008/937/EC concerning the non-inclusion of sulphuric acid in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I500520

Commission Decision No 2008/941/EC concerning the non-inclusion of certain active substances in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing these substances.

I40521

Commission Decision No 2008/943/EC concerning the non-inclusion of bone oil in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I220522

Commission Decision No 2008/953/EC recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Aureobasidium pullulans and disodium phosphonate in Annex I to Council Directive 91/414/EEC.

I456523

Commission Decision No 2008/967/EC concerning the non-inclusion of carbon monoxide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I392524

Commission Decision No 2008/986/EC concerning the non-inclusion of antraquinone in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I377525

Commission Decision No 2009/9/EC concerning the non-inclusion of nicotine in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I584526

Commission Decision No 2009/241/EC concerning the non-inclusion of triflumuron in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I476527

Commission Decision No 2009/311/EC allowing Member States to extend provisional authorisations granted for the new active substances topramezone, sulfuryl fluoride and zucchini yellow mosaic virus — weak strain.

I564528

Commission Decision No 2009/438/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of orange oil in Annex I to Council Directive 91/414/EEC.

I10529

Commission Decision No 2009/464/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of fluopyram in Annex I to Council Directive 91/414/EEC.

I443530

Commission Decision No 2009/535/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of BAS 650 F in Annex I to Council Directive 91/414/EEC.

I428531

Commission Decision No 2009/562/EC concerning the non-inclusion of metam in Annex I to Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I533532

Commission Decision No 2009/616/EC concerning the non-inclusion of petroleum oil CAS 92062-35-6 in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I359533

Commission Decision No 2009/617/EC concerning the non-inclusion of paraffin oil CAS 64742-54-7 in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I313534

Commission Decision No 2009/700/EC recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of bixafen in Annex I to Council Directive 91/414/EEC.

I581535

Commission Decision No 2009/715/EC concerning the non-inclusion of chlorthal-dimethyl in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I504536

Commission Decision No 2009/860/EC concerning the non-inclusion of triazoxide in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I495537

Commission Decision No 2009/865/EC allowing Member States to extend provisional authorisations granted for the new active substances metaflumizone and gamma-cyhalothrin.

I12538

Commission Decision No 2009/887/EC concerning the non-inclusion of bifenthrin in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance.

I243539

Commission Decision No 2010/132/EU recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of Trichoderma asperelleum (strain T34) and isopyrazam in Annex I to Council Directive 91/414/EEC.

I306540

Commission Decision No 2010/149/EU allowing Member States to extend provisional authorisations granted for the new active substances flonicamid, silver thiosulphate and tembotrione.

I505541

Commission Decision No 2010/150/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of fenpyrazamine in Annex I to Council Directive 91/414/EEC.

I589542

Commission Decision No 2010/164/EU recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of tagetes oil and thyme oil in Annex I of Council Directive 91/414/EEC.

I404543

Commission Decision No 2010/206/EU allowing Member States to extend provisional authorisations granted for the new active substance FEN 560.

I44544

Commission Decision No 2010/244/EU recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of 1,4-dimethylnapthalene and cyflumetofen in Annex I to Council Directive 91/414/EEC.

I452545

Commission Decision No 2010/353/EU allowing Member States to extend provisional authorisations granted for the new active substances amisulbrom, chlorantraniliprole, meptyldinocap and pinoxaden.

I563546

Commission Decision No 2010/355/EU concerning the non-inclusion of trifluralin in Annex I to Council Directive 91/414/EEC.

I309547

Commission Decision No 2010/356/EU allowing Member States to extend provisional authorisations granted for the new active substance profoxydim.

I134548

Commission Decision No 2010/455/EU amending Decisions 2008/934/EC and 2008/941/EC as regards the date until which authorisations may continue to be in force at 31.12.2020 and the period of grace, in cases where the notifier has submitted an application in accordance with the accelerated procedure under Regulation (EC) No 33/2008.

I522549

Commission Decision No 2010/457/EU allowing Member States to extend provisional authorisations granted for the new active substances Candida oleophila strain O, potassium iodide and potassium thiocyanate.

I201550

Commission Decision No 2010/466/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of penthiopyrad in Annex I of Council Directive 91/414/EEC.

I480551

Commission Decision No 2010/672/EU recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of penflufen and fluxapyroxad in Annex I to Council Directive 91/414/EEC.

I537552

Commission Decision No 2010/785/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of pyriofenone in Annex I to Council Directive 91/414/EEC.

I150553

Commission Decision No 2011/36/EU concerning the non-inclusion of 1,3-dichloropropene in Annex I to Council Directive 91/414/EEC.

I527554

Commission Decision No 2011/120/EU concerning the non-inclusion of methyl bromide in Annex I to Council Directive 91/414/EEC.

I532555

Commission Decision No 2011/123/EU recognising in principle the completeness of the dossiers submitted for detailed examination in view of the possible inclusion of sedaxane and Bacillus firmus I-1582 in Annex I to Council Directive 91/414/EEC.

I140556

Commission Decision No 2011/124/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of ethametsulfuron in Annex I to Council Directive 91/414/EEC.

I230557

Commission Decision No 2011/143/EU concerning the non-inclusion of ethoxyquin in Annex I to Council Directive 91/414/EEC and amending Commission Decision 2008/941/EC.

I241558

Commission Implementing Decision No 2011/234/EU concerning the non-inclusion of dichlobenil in Annex I to Council Directive 91/414/EEC.

I278559

Commission Implementing Decision No 2011/252/EU allowing Member States to extend provisional authorisations granted for the new active substances ascorbic acid, ipconazole, spiromesifen, topramezone, and Pseudomonas sp. strain DSMZ 13134.

I337560

Commission Implementing Decision No 2011/253/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of metobromuron, S-Abscisic acid, Bacillus amyloliquefaciens subsp. plantarum D747, Bacillus pumilus QST 2808 and Streptomyces lydicus WYEC 108 in Annex I to Council Directive 91/414/EEC.

I513561

Commission Implementing Decision No 2011/262/EU concerning the non-inclusion of propisochlor in Annex I to Council Directive 91/414/EEC and amending Commission Decision 2008/941/EC.

I321562

Commission Implementing Decision No 2011/266/EU recognising in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of beta-cypermethrin, eugenol, geraniol and thymol in Annex I to Council Directive 91/414/EEC.

I151563

Commission Implementing Decision No 2011/328/EU concerning the non-inclusion of flurprimidol in Annex I to Council Directive 91/414/EEC.

I521564

Commission Implementing Decision No 2011/329/EU concerning the non-inclusion of dicloran in Annex I to Council Directive 91/414/EEC.

I465565

Commission Implementing Decision No 2011/671/EU allowing Member States to extend provisional authorisations granted for the new active substances benalaxyl-M, gamma-cyhalothrin and valifenalate.

I520566

Commission Implementing Decision No 2012/187/EU amending Decision 2001/861/EC as regards novaluron.

I531567

Commission Implementing Decision of 6 June 2018 on the establishment of a work programme for the assessment of applications for the renewal of approvals of active substances expiring in 2022, 2023 and 2024 in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council.

(This note is not part of the Regulations)

These Regulations are made in exercise of the powers conferred by section 8(1) of the European Union (Withdrawal) Act 2018 (c. 16) in order to address failures of retained EU law to operate effectively and other deficiencies (in particular under section 8(2)(a), (b), (c), (d), (f) and (g)) arising from the withdrawal of the UK from the European Union.

These Regulations make amendments to legislation in the field of pesticides, and in particular amend legislation relating to plant protection products. Part 2 amends Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market and other supporting retained direct EU legislation. Part 3 transfers functions from Directive 2009/128/EC of the European Parliament and of the Council establishing a framework for Community action to achieve the sustainable use of pesticides (OJ No L 309, 24.11.2009, p 71). Part 4 makes consequential amendments, contains transitional provisions and savings, and revokes retained direct EU legislation.

An impact assessment has not been produced for this instrument as no, or no significant, impact on the private or voluntary sector is foreseen.