Commission Implementing Decision (EU) 2019/1304Dangos y teitl llawn

Commission Implementing Decision (EU) 2019/1304

of 26 July 2019

authorising the placing on the market of products containing, consisting of or produced from genetically modified maize 4114 (DP-ØØ4114-3), pursuant to Regulation (EC) No 1829/2003 of the European Parliament and of the Council

(notified under document C(2019) 5491)

(Only the Dutch and French texts are authentic)

(Text with EEA relevance)

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EC) No 1829/2003 of the European Parliament and of the Council of 22 September 2003 on genetically modified food and feed(1), and in particular to Articles 7(3) and 19(3) thereof,

Whereas:

(1) On 27 November 2014, Pioneer Overseas Corporation, on behalf of Pioneer Hi-Bred International Inc., United States, submitted to the national competent authority of the Netherlands an application in accordance with Articles 5 and 17 of Regulation (EC) No 1829/2003 (‘the application’). The application covered the placing on the market of foods, food ingredients and feed containing, consisting of or produced from genetically modified maize 4114. The application also covered the placing on the market of products containing or consisting of genetically modified maize 4114 for uses other than food and feed, with the exception of cultivation.

(2) In accordance with Articles 5(5) and 17(5) of Regulation (EC) No 1829/2003, the application included information and conclusions about the risk assessment carried out in accordance with the principles set out in Annex II to Directive 2001/18/EC of the European Parliament and of the Council(2). It also included the information required pursuant to Annexes III and IV to that Directive and a monitoring plan for environmental effects in accordance with Annex VII to that Directive.

(3) On 24 May 2018, the European Food Safety Authority (‘the Authority’) issued a favourable opinion in accordance with Articles 6 and 18 of Regulation (EC) No 1829/2003(3). The Authority concluded that genetically modified maize 4114, as described in the application, is as safe as the non-GM comparator(s) and the tested non-genetically modified maize reference varieties with respect to potential effects on human and animal health and the environment.

(4) In its opinion, the Authority considered all the questions and concerns raised by the Member States in the context of the consultation of the national competent authorities as provided for in Articles 6(4) and 18(4) of Regulation (EC) No 1829/2003.

(5) The Authority also concluded that the monitoring plan for environmental effects consisting of a general surveillance plan, submitted by the applicant, is in line with the intended uses of the products.

(6) Taking those considerations into account, the placing on the market of products containing, consisting of or produced from genetically modified maize 4114 should be authorised for the uses listed in the application.

(7) A unique identifier should be assigned to genetically modified maize 4114 in accordance with Commission Regulation (EC) No 65/2004(4).

(8) On the basis of the Authority's opinion, no specific labelling requirements, other than those provided for in Articles 13(1) and 25(2) of Regulation (EC) No 1829/2003 and in Article 4(6) of Regulation (EC) No 1830/2003 of the European Parliament and of the Council(5), appear to be necessary for the products covered by this Decision. However, in order to ensure that the use of those products remains within the limits of the authorisation granted by this Decision, the labelling of the products containing or consisting of genetically modified maize 4114, with the exception of foods and food ingredients, should contain a clear indication that they are not intended for cultivation.

(9) In order to account for the implementation and the results of the activities set out in the monitoring plan for environmental effects, the authorisation holder should submit annual reports, presented in accordance with the standard reporting format requirements laid down in Commission Decision 2009/770/EC(6).

(10) The opinion of the Authority does not justify the imposition of specific conditions or restrictions for the placing on the market, for the use and handling, including post-market monitoring requirements regarding the consumption of the food and feed, or for the protection of particular ecosystems/environment or geographical areas, as provided for in Article 6(5)(e) and Article 18(5)(e) of Regulation (EC) No 1829/2003.

(11) All relevant information on the authorisation of the products should be entered in the Community register of genetically modified food and feed referred to in Article 28(1) of Regulation (EC) No 1829/2003.

(12) This Decision is to be notified through the Biosafety Clearing-House to the Parties to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity, pursuant to Article 9(1) and Article 15(2)(c) of Regulation (EC) No 1946/2003 of the European Parliament and of the Council(7).

(13) The Standing Committee on Plants, Animals, Food and Feed has not delivered an opinion within the time limit laid down by its Chairman. This implementing act was deemed to be necessary and the chair submitted it to the appeal committee for further deliberation. The appeal committee did not deliver an opinion,

HAS ADOPTED THIS DECISION:

Article 1 U.K. Genetically modified organism and unique identifier

Genetically modified maize (Zea mays L.) 4114, as specified in point (b) of the Annex to this Decision, is assigned the unique identifier DP-ØØ4114-3, in accordance with Regulation (EC) No 65/2004.

Article 2 U.K. Authorisation

The following products are authorised for the purposes of Articles 4(2) and 16(2) of Regulation (EC) No 1829/2003 in accordance with the conditions set out in this Decision:

(a)

foods and food ingredients containing, consisting of or produced from genetically modified maize 4114;

(b)

feed containing, consisting of or produced from genetically modified maize 4114;

(c)

products containing or consisting of genetically modified maize 4114 for uses other than those provided for in points (a) and (b), with the exception of cultivation.

Article 3 U.K. Labelling

1. For the purposes of the labelling requirements laid down in Articles 13(1) and 25(2) of Regulation (EC) No 1829/2003 and in Article 4(6) of Regulation (EC) No 1830/2003, the ‘name of the organism’ shall be ‘maize’.

2. The words ‘not for cultivation’ shall appear on the label of and in the documents accompanying products containing or consisting of genetically modified maize 4114, with the exception of foods and food ingredients.

Article 4 U.K. Method for detection

The method set out in point (d) of the Annex shall apply for the detection of genetically modified maize 4114.

Article 5 U.K. Monitoring for environmental effects

1. The authorisation holder shall ensure that the monitoring plan for environmental effects, as set out in point (h) of the Annex, is put in place and implemented.

2. The authorisation holder shall submit to the [F1 Food Safety Authority] annual reports on the implementation and the results of the activities set out in the monitoring plan in accordance with Decision 2009/770/EC.

Textual Amendments

F1 Words in Art. 5(2) substituted (31.12.2020) by The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 410 (as inserted by S.I. 2020/1504, regs. 1(2), 17(21)); 2020 c.1, Sch. 5 para. 1(1)

Article 6 U.K. [F2 Register]

The information set out in the Annex to this Decision shall be entered in the F3 ... register of genetically modified food and feed referred to in Article 28(1) of Regulation (EC) No 1829/2003.

Textual Amendments

F2 Art. 6 heading substituted (31.12.2020) by The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 411 (as inserted by S.I. 2020/1504, regs. 1(2), 17(21)); 2020 c.1, Sch. 5 para. 1(1)

F3 Word in Art. 6 omitted (31.12.2020) by virtue of The Genetically Modified Food and Feed (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/705), regs. 1, 412 (as inserted by S.I. 2020/1504, regs. 1(2), 17(21)); 2020 c.1, Sch. 5 para. 1(1)

Article 7 U.K. Authorisation holder

 [F4 The authorisation holder is Corteva Agriscience LLC, United States of America, represented in Great Britain by Corteva Agriscience UK Limited.]

Textual Amendments

F4 Words in Art. 7 substituted: (E.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (England) Regulations 2023 (S.I. 2023/235), regs. 1(b), 18(2); (S.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Scotland) Regulations 2023 (S.S.I. 2023/59), regs. 1(1), 18(2); and (W.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Wales) Regulations 2023 (S.I. 2023/379), regs. 1(2)(c), 18(2)

Article 8 U.K. Validity

This Decision shall apply for a period of 10 years from the date of its notification.

Article 9 U.K. Addressee

 [F5 This Decision is addressed to Corteva Agriscience LLC, 9330 Zionsville Road, Indianapolis, Indiana, 46268-1054, United States of America, represented in Great Britain by Corteva Agriscience UK Limited, Cpc2 Capital Park, Fulbourn, Cambridge, England, CB21 5XE.]

Textual Amendments

F5 Words in Art. 9 substituted: (E.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (England) Regulations 2023 (S.I. 2023/235), regs. 1(b), 18(3); (S.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Scotland) Regulations 2023 (S.S.I. 2023/59), regs. 1(1), 18(3); and (W.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Wales) Regulations 2023 (S.I. 2023/379), regs. 1(2)(c), 18(3)

Done at Brussels, 26 July 2019.

For the Commission

Vytenis Andriukaitis

Member of the Commission

ANNEX U.K.

(a) [F6 Authorisation holder: U.K.

(1)

The authorisation holder is Corteva Agriscience LLC, 9330 Zionsville Road, Indianapolis, Indiana, 46268-1054, United States of America.

(2)

The authorisation holder is represented in Great Britain by Corteva Agriscience UK Limited, Cpc2 Capital Park, Fulbourn, Cambridge, England, CB21 5XE.]

Textual Amendments

F6 Annex point (a) substituted: (E.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (England) Regulations 2023 (S.I. 2023/235), regs. 1(b), 18(4); (S.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Scotland) Regulations 2023 (S.S.I. 2023/59), regs. 1(1), 18(4); and (W.) (26.4.2023) by The Genetically Modified Food and Feed (Authorisations and Modifications of Authorisations) (Wales) Regulations 2023 (S.I. 2023/379), regs. 1(2)(c), 18(4)

(b) Designation and specification of the products: U.K.

(1)

foods and food ingredients containing, consisting of or produced from genetically modified maize 4114;

(2)

feed containing, consisting of or produced from genetically modified maize 4114;

(3)

products containing or consisting of genetically modified maize 4114 for uses other than those provided for in points (1) and (2), with the exception of cultivation.

The genetically modified maize 4114 expresses the Cry1F (truncated version), Cry34Ab1 and Cry35Ab1 proteins providing protection against specific lepidopteran and coleopteran pests, and the PAT protein conferring tolerance to glufosinate-ammonium based herbicides.

(c) Labelling: U.K.

(1)

For the purposes of the labelling requirements laid down in Article 13(1) and Article 25(2) of Regulation (EC) No 1829/2003, and in Article 4(6) of Regulation (EC) No 1830/2003, the ‘name of the organism’ shall be ‘maize’.

(2)

The words ‘not for cultivation’ shall appear on the label of and in documents accompanying the products containing or consisting of genetically modified maize 4114, with the exception of products referred to in point (b)(1) of this Annex.

(d) Method for detection: U.K.

(1)

Event-specific real-time quantitative PCR based method for detection of the genetically modified maize DP-ØØ4114-3.

(2)

Validated by the EU reference laboratory established under Regulation (EC) No 1829/2003, published at http://gmo-crl.jrc.ec.europa.eu/StatusOfDossiers.aspx

(3)

Reference Material: ERM®-BF439 is accessible via the Joint Research Centre (JRC) of the European Commission at https://ec.europa.eu/jrc/en/reference-materials/catalogue/

(e) Unique identifier: U.K.

DP-ØØ4114-3

(f) Information required under Annex II to the Cartagena Protocol on Biosafety to the Convention on Biological Diversity: U.K.

[Biosafety Clearing-House, Record ID number: published in the register of genetically modified food and feed when notified].

(g) Conditions or restrictions on the placing on the market, use or handling of the products: U.K.

Not required.

(h) Monitoring plan for environmental effects: U.K.

Monitoring plan for environmental effects in accordance with Annex VII to Directive 2001/18/EC.

[Link: plan published in the register of genetically modified food and feed]

(i) Post-market monitoring requirements for the use of the food for human consumption: U.K.

Not required.

Note: links to relevant documents may need to be modified over the time. Those modifications will be made available to the public via the updating of the register of genetically modified food and feed. U.K.

(1)

OJ L 268, 18.10.2003, p. 1.

(2)

Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms and repealing Council Directive 90/220/EEC (OJ L 106, 17.4.2001, p. 1).

(3)

EFSA GMO Panel (EFSA Panel on Genetically Modified Organisms), 2018. Scientific Opinion on the assessment of genetically modified maize 4114 for food and feed uses, under Regulation (EC) No 1829/2003 (application EFSA-GMO-NL-2014-123). EFSA Journal 2018; 16(5):5280, 25 pp. https://doi.org/10.2903/j.efsa.2018.5280

(4)

Commission Regulation (EC) No 65/2004 of 14 January 2004 establishing a system for the development and assignment of unique identifiers for genetically modified organisms (OJ L 10, 16.1.2004, p. 5).

(5)

Regulation (EC) No 1830/2003 of the European Parliament and of the Council of 22 September 2003 concerning the traceability and labelling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms and amending Directive 2001/18/EC (OJ L 268, 18.10.2003, p. 24).

(6)

Commission Decision 2009/770/EC of 13 October 2009 establishing standard reporting formats for presenting the monitoring results of the deliberate release into the environment of genetically modified organisms, as or in products, for the purpose of placing on the market, pursuant to Directive 2001/18/EC of the European Parliament and of the Council (OJ L 275, 21.10.2009, p. 9).

(7)

Regulation (EC) No 1946/2003 of the European Parliament and of the Council of 15 July 2003 on transboundary movements of genetically modified organisms (OJ L 287, 5.11.2003, p. 1).