OpenLegislation

Division 6 F1

United Kingdom

Original text. Later amendments are not shown.

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

Textual amendments

F1

Substituted by Commission Directive 2009/9/EC of 10 February 2009 amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use (Text with EEA relevance).

Footnotes

f1

OJ L 50, 20.2.2004, p. 44 .

f2

OJ L 50, 20.2.2004, p. 28 .