# 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: Applications shall contain all the necessary information to allow the appropriate authority to assess the safety of the proposed alternative method, and in particular describe:

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

the categories of animal by-products intended to be submitted to the method,
the entire process,
the biological hazards for human and animal health involved, and
the degree of risk reduction to be achieved by the process.

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