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Regulation (EC) No 1774/2002 of the European Parliament and of the Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption (repealed)
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Version Superseded: 04/03/2011
Point in time view as at 07/08/2009. This version of this provision has been superseded.
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1.Member States may authorise, under the supervision of the competent authorities:
(a)the use of animal by-products for diagnostic, educational and research purposes; and
(b)the use of animal by-products for taxidermy purposes in technical plants approved for this purpose in accordance with Article 18.
2.(a)Member States may also authorise the use of the animal by-products specified in subparagraph (b) for the feeding of the animals specified in subparagraph (c), under the supervision of the competent authorities and in accordance with the rules laid down in Annex IX.
(b)The animal by-products referred to in subparagraph (a) are:
Category 2 material, provided that it comes from animals which were not killed or did not die as a result of the presence or suspected presence of a disease communicable to humans or animals, and
Category 3 material referred to in Article 6(1)(a) to (j) and, subject to Article 22, in Article 6(1)(l).
(c)The animals referred to in subparagraph (a) are:
zoo animals,
circus animals,
reptiles and birds of prey other than zoo or circus animals,
fur animals,
wild animals the meat of which is not destined for human consumption,
dogs from recognised kennels or packs of hounds, and
maggots for fishing bait.
[F1(d) In addition, Member States may authorise the use, under the supervision of the competent authorities, of Category 1 material referred to in Article 4(1)(b)(ii) for the feeding of endangered or protected species of necrophagous birds in accordance with rules laid down by the Commission after consultation of the European Food Safety Authority. Those measures, designed to amend non-essential elements of this Regulation by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 33(3).]
3.Member States shall inform the Commission of:
(a)the use made of the derogations referred to in paragraph 2; and
(b)the verification arrangements introduced to ensure that the animal by-products concerned are used only for authorised purposes.
4.Each Member State shall draw up a list of users and collection centres authorised and registered pursuant to paragraph 2(c)(iv), (vi) and (vii) within its territory. Each user and collection centre shall be assigned an official number for inspection purposes and to be able to trace the origin of the products concerned.
The competent authority shall supervise the premises of users and collection centres referred to in the previous subparagraph and have free access at all times to all parts of such premises, to ensure compliance with the requirements referred to in paragraph 2.
If such inspections reveal that those requirements are not being complied with, the competent authority shall take appropriate action.
[F15. Detailed rules concerning verification measures may be adopted by the Commission. Those measures, designed to amend non-essential elements of this Regulation by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 33(3).]
Textual Amendments
F1 Substituted by Regulation (EC) No 596/2009 of the European Parliament and of the Council of 18 June 2009 adapting a number of instruments subject to the procedure referred to in Article 251 of the Treaty to Council Decision 1999/468/EC with regard to the regulatory procedure with scrutiny Adaptation to the regulatory procedure with scrutiny — Part Four.
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