# 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), Division 1: Operators shall ensure that consignments of research and diagnostic samples are accompanied by a commercial document, which must specify:

Extent: E+W+S+N.I.

(a)the description of the material and the animal species of origin;
(b)the category of the material;
(c)the quantity of the material;
(d)the place of origin and the place of dispatch of the material;
(e)the name and the address of the consignor;
(f)the name and the address of the consignee and/or user.

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Source: https://www.legislation.gov.uk/eur/2011/142/annex/VI/chapter/I/section/1/division/1 (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-142/annex-VI/chapter-I/section-1/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.