OpenLegislation

Division 6

United Kingdom

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^f1 and Directive 2004/9/EC of the European Parliament and of the Council^f2.

Annotations

Footnotes

f1: OJ L 50, 20.2.2004, p. 44.
f2: OJ L 50, 20.2.2004, p. 28.

Notes on Annex II

Footnotes

f1: This Annex will be amended by the Commission in accordance with Articles 146 and 153. All references to Articles or to ‘this Directive’ in this Annex, unless otherwise specified, are to be understood as references to Directive 2001/82/EC.