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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)
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Unless they are kept for reference purposes or redispatched to the third country of origin, research and diagnostic samples and any products derived from the use of those samples shall be disposed of:
as waste by incineration;
by pressure sterilisation and subsequent disposal or use in accordance with Articles 12 to 14 of Regulation (EC) No 1069/2009; or
in accordance with point 4(b) of Section 1 of Chapter I of Annex VI in case:
of quantities not exceeding 2 000 ml; and
provided the samples or derived products have been produced in and dispatched from third countries F1..., which are listed in Part I of Annex II to Regulation (EU) No 206/2010 [F2, or territories or parts of those third countries, from which imports into Great Britain of fresh meat of domestic bovine animals are authorised by virtue of being 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].
Textual Amendments
F1Words in Annex 14 Ch. 3 Section 1 point (c)(ii) 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(4)(a)(i)
F2Words in Annex 14 Ch. 3 Section 1 point (c)(ii) 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(4)(a)(ii)
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