OpenLegislation

Chapter 3 RISK MANAGEMENT CONSIDERATIONS

United Kingdom

Original text. Later amendments are not shown.

Based on the risk assessment performed, relevant risk management recommendations in accordance with Article 7 of Regulation (EC) No 470/2009 shall be addressed, in particular:

  • other legitimate factors such as technological aspects of food and feed productions, feasibility of controls, conditions of use and application of the substances in veterinary medicinal products;

  • other relevant risk management considerations for the establishment of MRLs;

  • elaboration of MRLs;

  • considerations on possible extrapolation of MRLs.

Notes on Annex

Textual amendments

F1

Words in Annex para. 2 substituted (31.12.2020) by The Veterinary Medicines and Animals and Animal Products (Examination of Residues and Maximum Residue Limits) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/676), regs. 1(2)(b), 8(5)(a); 2020 c. 1, Sch. 5 para. 1(1)

Footnotes

f1

Directive 2004/10/EC of the European Parliament and of the Council of 11 February 2004 on the harmonisation of laws, regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their applications for tests on chemical substances (OJ L 50, 20.2.2004, p. 44).

f2

Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the protection of animals used for scientific purposes (OJ L 276, 20.10.2010, p. 33).