OpenLegislation

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:F1F2

United Kingdom

Original text. Later amendments are not shown.

  • 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.

Annotations

Textual amendments

F1

Substituted by Commission Regulation (EU) No 749/2011 of 29 July 2011 amending Regulation (EU) No 142/2011 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).

F2

Words in Annex 7 Ch. 2 para. 1 substituted (E.W.S.) (31.12.2020) by The Animals, Aquatic Animal Health, Invasive Alien Species, Plant Propagating Material and Seeds (Amendment) (EU Exit) Regulations 2020 (S.I. 2020/1388), regs. 1(2)(c), 13(45)(b)