# Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products, Division 6

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

Pharmacological, toxicological, residue and safety tests shall be carried out in conformity with the provisions related to Good Laboratory Practice (GLP) laid down in Directive 2004/10/EC of the European Parliament and of the Council and Directive 2004/9/EC of the European Parliament and of the Council .

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/division/1/division/6 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/division-1/division-6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.