# 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 4: A commercial document in accordance with the model made available or published for the time being by the appropriate authority shall accompany animal by-products and derived products as from the starting point in the manufacturing chain referred to in Article 4(1) of Regulation (EC) No 1069/2009, during transportation within Great Britain.

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

However, in addition to the authorisation to transmit information by way of an alternative system as referred to in the second subparagraph of Article 21(3) of Regulation (EC) No 1069/2009, the competent authority may authorise that animal by-products and derived products which are transported in its constituent nation are accompanied by:
(a)a different commercial document, in paper or in electronic form, provided that such commercial document contains the information referred to in point (f) of the Notes under point 6 of this Chapter;
(b)a commercial document in which the quantity of the material is expressed in weight or volume of the material or in the number of packages.

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Source: https://www.legislation.gov.uk/eur/2011/142/annex/VIII/chapter/III/division/4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2011-142/annex-VIII/chapter-III/division-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

