- Latest available (Revised)
- Original (As adopted by EU)
Commission Regulation (EU) No 142/2011 of 25 February 2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance)
When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.
Legislation.gov.uk publishes the UK version. EUR-Lex publishes the EU version. The EU Exit Web Archive holds a snapshot of EUR-Lex’s version from IP completion day (31 December 2020 11.00 p.m.).
There are currently no known outstanding effects for the Commission Regulation (EU) No 142/2011, Division CHAPTER I.
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
As referred to in Article 41(1)(a) and Article 41(3) of Regulation (EC) No 1069/2009, the following requirements shall apply to F3... consignments of Category 3 material and derived products therefrom [F4imported from a third country] for uses in the feed chain other than for petfood or for feed to fur animals and consignments of such materials and products in transit:
Textual Amendments
F3Word in Annex 14 Ch. 1 Section 1 omitted (E.W.S.) (31.12.2020) by virtue of The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(a)(i)
F4Words in Annex 14 Ch. 1 Section 1 inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(a)(ii)
they must consist of or have been produced from, as applicable, Category 3 material referred to in the column ‘raw materials’ of Table 1;
they must comply with the import and transit conditions set out in the column ‘import and transit conditions’ of Table 1;
[F5they must come from a third country or part of a third country listed in the column ‘ third countries’ list ’ of Table 1;
they must come from an establishment or plant which is registered or approved by the competent authority of the third country, as applicable, and which is on the list of such establishments and plants referred to in Article 30; and
they must be:
accompanied during transportation to the point of entry into [F6Great Britain] where the veterinary checks take place by the health certificate referred to in the column ‘ certificates/model documents ’ of Table 1; or
presented at the point of entry into [F7Great Britain] where the veterinary checks take place accompanied by a document corresponding to the model referred to in the column ‘ certificates/model documents ’ of Table 1.]
F8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Textual Amendments
F5Substituted by Commission Regulation (EU) No 294/2013 of 14 March 2013 amending and correcting Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance).
F6Words in Annex 14 Ch. 1 Section 1 point (e)(i) substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(b)
F7Words in Annex 14 Ch. 1 Section 1 point (e)(ii) substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(b)
F8Deleted by Commission Regulation (EU) No 294/2013 of 14 March 2013 amending and correcting Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance).
No | Product | Raw materials (reference to provisions of Regulation (EC) No 1069/2009) | Import and transit conditions | Third countries’ lists | Certificates/model documents |
---|---|---|---|---|---|
[F91 | Processed animal protein, including mixtures and products other than petfood containing such protein, and compound feeds containing such proteins as defined in Article 3(2)(h) of Regulation (EC) No 767/2009 | Category 3 materials referred to in Article 10(a), (b), (d), (e), (f), (h), (i), (j), (k), (l) and (m). | (a) The processed animal protein must have been produced in accordance with Section 1 of Chapter II of Annex X; and (b) the processed animal protein shall comply with the additional requirements set out in Section 2 of this Chapter. | (a) In the case of processed animal proteins excluding fishmeal: Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010. (b) In the case of fishmeal: Third countries listed in Annex II to [F10Commission Implementing Regulation (EU) 2019/626 concerning lists of third countries or regions thereof authorised for the entry into the European Union of certain animals and goods intended for human consumption]. | [F11The relevant health certificate made available or published for the time being by the appropriate authority.]] |
2 | Blood products for feed material | Category 3 materials referred to in Article 10 (a) and (b)(i). | [F12The blood products must have been produced in accordance with Section 2 of Chapter II of Annex X and Section 5 of Chapter I of Annex XIV.] | (a)In the case of blood products from ungulates:Third countries F13... listed in Part 1 of Annex II to Regulation (EU) No 206/2010 [F14, or territories or parts of those third countries, specified by the Secretary of State, with the consent of the Scottish Ministers (in relation to Scotland) and the Welsh Ministers (in relation to Wales), under Article 14 of that Regulation in a document published for the purposes of that Article], from which imports of all categories of fresh meat of the respective species are authorised. (b)In the case of blood products from other species:Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010. | [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
3 | Rendered fats and fish oil | (a)In the case of rendered fats excluding fish oil: Category 3 materials referred to in Article 10(a), (b), (d), (e), (f), (g), (h), (i), (j) and (k).(b)In the case of fish oil: Category 3 materials referred to in Article 10(e), (f), (i) and (j). | (a)The rendered fat and the fish oil must have been produced in accordance with Section 3 of Chapter II of Annex X; and(b)The rendered fat shall comply with the additional requirements set out in Section 3 of this Chapter. | (a)In the case of rendered fats excluding fish oil:Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010. (b)In the case of fish oil:Third countries listed in Annex II to [F10Commission Implementing Regulation (EU) 2019/626 concerning lists of third countries or regions thereof authorised for the entry into the European Union of certain animals and goods intended for human consumption]. | [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
4 | Milk, milk-based products and milk-derived products, colostrum, colostrum products | (a)Milk, milk-based products:Category 3 materials referred to in Article 10(e), (f) and (h). (b)Colostrum, colostrum productsCategory 3 materials from live animals that did not show any signs of disease transmissible through the colostrums to humans or animals. | The milk, milk-based products, colostrum and colostrum products shall comply with the requirements set out in Section 4 of this Chapter. | (a)In the case of milk and milk-based products:Authorised third countries listed in Annex I to Regulation (EU) No 605/2010. [F15(b) in the case of colostrum and colostrum products third countries listed in Annex 1 to Regulation (EU) No 605/2010 and specified by the Secretary of State, with the consent of the Scottish Ministers (in relation to Scotland) and the Welsh Ministers (in relation to Wales), under Article 2 of that Regulation in a document published for the purposes of that Article.] | [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
[F165 | Gelatine and hydrolysed protein | Category 3 materials referred to in Article 10(a), (b), (e), (f), (g), (i) and (j), and, in the case of hydrolysed protein: Category 3 materials referred to in Article 10(d), (h) and (k). | The gelatine and the hydrolysed protein must have been produced in accordance with Section 5 of Chapter II of Annex X. | (a) Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010, and the following countries:
(b) In the case of gelatine and hydrolysed proteins from fish: Third countries listed in Annex II to [F10Commission Implementing Regulation (EU) 2019/626 concerning lists of third countries or regions thereof authorised for the entry into the European Union of certain animals and goods intended for human consumption]. | [F11The relevant health certificate made available or published for the time being by the appropriate authority. ]] |
6 | Dicalcium phosphate | Category 3 materials referred to in Article 10(a), (b), (d),(e), (f), (g), (h), (i), (j) and (k). | The dicalcium phosphate must have been produced in accordance with Section 6 of Chapter II of Annex X. | Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010, and the following countries:
| [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
7 | Tricalcium phosphate | Category 3 materials referred to in Article 10(a), (b), (d),(e), (f), (g), (h), (i) and (k). | The tricalcium phosphate must have been produced in accordance with Section 7 of Chapter II of Annex X. | Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010, and the following countries:
| [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
8 | Collagen | Category 3 materials referred to in Article 10(a), (b), (e), (f), (g), (i) and (j). | The collagen must have been produced in accordance with Section 8 of Chapter II of Annex X. | Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010, and the following countries:
| [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
9 | Egg products | Category 3 materials referred to in Article 10(e), (f) and (k)(ii). | The egg products must have been produced in accordance with Section 9 of Chapter II of Annex X. | Third countries listed in Part 1 of Annex II to Regulation (EU) No 206/2010, and third countries F17... from which [F18imports into Great Britain] of fresh poultrymeat, eggs and egg products [F19are authorised], which are listed in Part 1 of Annex I to Regulation (EC) No 798/2008 [F20, or territories, zones or compartments of those third countries, specified by the Secretary of State, with the consent of the Scottish Ministers (in relation to Scotland) and the Welsh Ministers (in relation to Wales), under Article 3 of that Regulation in a document published for the purposes of that Article]. | [F11The relevant health certificate made available or published for the time being by the appropriate authority. ] |
Textual Amendments
F9Substituted by Commission Regulation (EU) 2017/893 of 24 May 2017 amending Annexes I and IV to Regulation (EC) No 999/2001 of the European Parliament and of the Council and Annexes X, XIV and XV to Commission Regulation (EU) No 142/2011 as regards the provisions on processed animal protein (Text with EEA relevance).
F10Words in Annex 14 Ch. 1 Section 1 Table 1 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(c)(i)
F11Words in Annex 14 Ch. 1 Section 1 Table 1 substituted (31.12.2020) by The Animals (Legislative Functions) (EU Exit) Regulations 2019 (S.I. 2019/588), regs. 1, 10(9)(a) (with reg. 12); 2020 c. 1, Sch. 5 para. 1(1)
F12Substituted by Commission Regulation (EU) 2015/9 of 6 January 2015 amending Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance).
F13Words in Annex 14 Ch. 1 Section 1 Table 1 omitted (1.7.2022) by virtue of The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(a)(i)(aa)
F14Words in Annex 14 Ch. 1 Section 1 Table 1 inserted (1.7.2022) by The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(a)(i)(bb)
F15Words in Annex 14 Ch. 1 Section 1 Table 1 substituted (1.7.2022) by The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(a)(ii)
F16Substituted by Commission Implementing Regulation (EU) 2019/1177 of 10 July 2019 amending Regulation (EU) No 142/2011 as regards imports of gelatine, flavouring innards and rendered fats (Text with EEA relevance).
F17Words in Annex 14 Ch. 1 Section 1 Table 1 omitted (1.7.2022) by virtue of The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(a)(iii)(aa)
F18Words in Annex 14 Ch. 1 Section 1 Table 1 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(c)(ii)(aa)
F19Words in Annex 14 Ch. 1 Section 1 Table 1 inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(73)(c)(ii)(bb)
F20Words in Annex 14 Ch. 1 Section 1 Table 1 inserted (1.7.2022) by The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(a)(iii)(bb)
The following requirements shall apply to the importation [F23from a third country] of processed animal protein:
Textual Amendments
F23Words in Annex 14 Ch. 1 Section 2 inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(b)
Before consignments are released for free circulation within [F24Great Britain], the competent authority must sample processed animal protein from imported consignments at the [F25border control post] to ensure compliance with the general requirements of Chapter I of Annex X.
The competent authority must:
sample each consignment of products carried in bulk;
carry out random sampling of consignments of products packaged in the manufacturing plant of origin.
By way of derogation from point 1, when six consecutive tests on bulk consignments originating in a given third country prove negative, the competent authority of the [F25border control post] may carry out random sampling of subsequent bulk consignments from that third country.
If one of those random samples proves positive, the competent authority carrying out the sampling must inform the competent authority of the third country of origin so that it can take appropriate measures to remedy the situation.
The competent authority of the third country of origin must bring these measures to the attention of the competent authority carrying out the sampling.
In the event of a further positive result from the same source, the competent authority of the [F25border control post] must sample each consignment from the same source until six consecutive tests again prove negative.
Competent authorities must keep a record for at least three years of the results of sampling carried out on all consignments that have undergone sampling.
Where a consignment imported into [F26Great Britain] proves to be positive for salmonella or where it does not meet the microbiological standards for enterobacteriaceae set out in Chapter I of Annex X, it must either:
be dealt with in accordance with the procedure laid down by [F27Article 66(3)(b), 69 and 72 of the Official Controls Regulation]; or
reprocessed in a processing plant or decontaminated by a treatment authorised by the competent authority. The consignment must not be released until it has been treated, tested for salmonella or enterobacteriaceae, as necessary, by the competent authority in accordance with Chapter I of Annex X, and a negative result obtained.
[F28Processed animal protein obtained from farmed insects may be imported into [F29Great Britain] provided that it has been produced in compliance with the following conditions:
the insects belong to one of the following species:
Black Soldier Fly ( Hermetia illucens ) and Common Housefly ( Musca domestica ),
Yellow Mealworm ( Tenebrio molitor ) and Lesser Mealworm ( Alphitobius diaperinus ),
House cricket ( Acheta domesticus ), Banded cricket ( Gryllodes sigillatus ) and Field Cricket ( Gryllus assimilis );
the substrate for the feeding of insects may only contain products of non-animal origin or the following products of animal origin of Category 3 material:
fishmeal,
blood products from non-ruminants,
di and tricalcium phosphate of animal origin,
hydrolysed proteins from non-ruminants,
hydrolysed proteins from hides and skins of ruminants,
gelatine and collagen from non-ruminants,
eggs and egg products,
milk, milk based-products, milk-derived products and colostrum,
honey,
rendered fats;
the substrate for the feeding of insects and the insects or their larvae have not been in contact with any other materials of animal origin than those mentioned in point (b) and the substrate did not contain manure, catering waste or other waste.]
Textual Amendments
F24Words in Annex 14 Ch. 1 Section 2 point 1 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(c)
F25Words in Regulation substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(2)(b)
F26Words in Annex 14 Ch. 1 Section 2 point 4 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(d)(i)
F27Words in Annex 14 Ch. 1 Section point 4(a) substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(d)(ii)
F28Inserted by Commission Regulation (EU) 2017/893 of 24 May 2017 amending Annexes I and IV to Regulation (EC) No 999/2001 of the European Parliament and of the Council and Annexes X, XIV and XV to Commission Regulation (EU) No 142/2011 as regards the provisions on processed animal protein (Text with EEA relevance).
F29Words in Annex 14 Ch. 1 Section 2 point 5 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(e)
Textual Amendments
F21Substituted by Commission Regulation (EU) No 749/2011 of 29 July 2011 amending Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance).
F22Words in Annex 14 Ch. 1 Section 2 heading inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(74)(a)
The following requirements shall apply to the importation [F31from a third country] of rendered fats:
Textual Amendments
F31Words in Annex 14 Ch. 1 Section 3 inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(75)(b)
Rendered fat shall:
be entirely or partly derived from porcine raw material and come from a third country or a part of the territory of a third country free from foot-and-mouth disease for the previous 24 months and free from classical swine fever and African swine fever for the previous 12 months;
be entirely or partly derived from poultry raw material and come from a third country or a part of the territory of a third country free from Newcastle disease and avian influenza for the previous six months;
be entirely or partly derived from ruminant raw material and come from a third country or a part of the territory of a third country free from foot-and-mouth disease for the previous 24 months and free from rinderpest for the previous 12 months; or
where there has been an outbreak of one of the diseases referred to in points (a), (b) and (c) during the relevant period referred to in those points, have been subjected to one of the following heat treatments:
at least 70 °C for at least 30 minutes; or
at least 90 °C for at least 15 minutes.
Details of the critical control points shall be recorded by operators and maintained so that the owner, operator or their representative and, as necessary, the competent authority can monitor the operation of the plant; and the recorded information shall include the particle size, critical temperature and, as appropriate, the absolute time, pressure profile, raw material feed rate and fat recycling rate.
Textual Amendments
F30Words in Annex 14 Ch. 1 Section 3 heading inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(75)(a)
Milk, milk-based products and milk-derived products shall:
have undergone at least one of the treatments provided for in points 1.1, 1.2, 1.3 and point (a) of point B.1.4 of Part I of Section 4 of Chapter II of Annex X;
comply with points B.2 and B.4, and, in the case of whey, point B.3 of Part I of Section 4 of Chapter II of Annex X.
By way of derogation from point B.1.4 of Part I of Section 4 of Chapter II of Annex X, milk, milk-based products and milk-derived products may be imported from third countries [F34, or parts of those third countries, specified by the Secretary of State, with the consent of the Scottish Ministers (in relation to Scotland) and the Welsh Ministers (in relation to Wales), under Article 2 of] Regulation (EU) No 605/2010 [F35in a document published for the purposes of that Article], provided that the milk, milk-based products or milk-derived products have undergone a single HTST treatment and:
have not been shipped before a period of at least 21 days has elapsed after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country; or
Textual Amendments
F34Words in Annex 14 Ch. 1 Section 4 point A(2) substituted (1.7.2022) by The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(b)(i)
F35Words in Annex 14 Ch. 1 Section 4 point A(2) inserted (1.7.2022) by The Import of Animals and Animal Products and Approved Countries (Amendment) Regulations 2022 (S.I. 2022/735), regs. 1(2), 7(2)(b)(ii)
F36Words in Annex 14 Ch. 1 Section 4 point A(2)(b) substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(b)(ii)
Textual Amendments
F33Words in Annex 14 Ch. 1 Section 4 point A inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(b)(i)
The materials shall have undergone a single HTST treatment and:
have not been shipped before a period of at least 21 days has elapsed after production and during that period no case of foot-and-mouth disease has been detected in the exporting third country; or
The materials shall have been obtained from bovine animals subject to regular veterinary inspections to ensure that they come from holdings on which all bovine herds are:
either recognised as officially tuberculosis-free and officially brucellosis-free as defined in Article 2(2)(d) and (f) of Directive 64/432/EEC [F39taken with the Annexes to which they refer, reading the relevant provisions as if for references to a “Member State” or “Member States” there were substituted references to a “third country” or “third countries” (as the case may be)] or not restricted under the national legislation of the third country of origin of the colostrum regarding eradication of tuberculosis and brucellosis; and
either recognised as official enzootic-bovine-leukosis-free as defined in Article 2(2)(j) of Directive 64/432/EEC [F40taken with the Annex to which it refers, reading the relevant provisions as if:
for references to a “Member State” or “Member States” there were substituted references to a “third country” or “third countries” (as the case may be); and
in Annex D, in Chapter 1, in Section B(iv), for the reference to “Directive 72/462/EEC” there were substituted a reference to “Regulation (EU) 2017/625 on official controls and other official activities performed to ensure the application of food and feed law, rules on animal health and welfare, plant health and plant protection products and the Trade in Animals and Related Products Regulations 2011, the Trade in Animals and Related Products (Wales) Regulations 2011 or the Trade in Animals and Related Products (Scotland) Regulations 2012”;]
or included in an official system for the control of enzootic bovine leukosis and there has been no evidence as a result of clinical and laboratory testing of this disease in the herd during the past two years.
After completion of the processing, every precaution shall have been taken to prevent contamination of the colostrum or colostrum products.
The final product must bear a label so as to indicate that it contains Category 3 material and is not intended for human consumption, and it must have been:
packed in new containers; or
transported in bulk in containers or other means of transport that before use were thoroughly cleaned and disinfected.
Textual Amendments
F38Words in Annex 14 Ch. 1 Section 4 point B(1)(b) substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(c)(ii)
F39Words in Annex 14 Ch. 1 Section 4 point B(2)(a) inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(c)(iii)(aa)
F40Annex 14 Ch. 1 Section 4 point B(2)(b)(i)(ii) and words inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(c)(iii)(bb)
Textual Amendments
F37Words in Annex 14 Ch. 1 Section 4 point B inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(c)(i)
Textual Amendments
F32Words in Annex 14 Ch. 1 Section 4 heading inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(76)(a)
The following requirements shall apply to the importation [F43from a third country] of blood products, including spray dried blood and blood plasma which have been derived from porcine animals intended for the feeding of porcine animals:
Textual Amendments
F43Words in Annex 14 Ch. 1 Section 5 inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(77)(b)
These derived products must be:
subjected to a heat treatment at a temperature of at least 80 °C throughout the substance and the dry blood and blood plasma is of not more than 8 % moisture with a water activity (Aw) of less than 0,60;
stored in dry warehouse conditions under room temperature for at least 6 weeks.]
Textual Amendments
F41Inserted by Commission Regulation (EU) 2015/9 of 6 January 2015 amending Regulation (EU) No 142/2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance).
F42Words in Annex 14 Ch. 1 Section 5 heading inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(77)(a)
Textual Amendments
F1Words in Annex 14 Ch. 1 heading inserted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(72)(a)
F2Words in Annex 14 Ch. 1 heading substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(72)(b)
The Whole Regulation you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
The Schedules you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
This timeline shows the different versions taken from EUR-Lex before exit day and during the implementation period as well as any subsequent versions created after the implementation period as a result of changes made by UK legislation.
The dates for the EU versions are taken from the document dates on EUR-Lex and may not always coincide with when the changes came into force for the document.
For any versions created after the implementation period as a result of changes made by UK legislation the date will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. For further information see our guide to revised legislation on Understanding Legislation.
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including: