OpenLegislation

Division (9) F1

United Kingdom

Original text. Later amendments are not shown.

Non-clinical (pharmaco-toxicological) studies shall be carried out in conformity with the provisions related to Good Laboratory Practice laid down in Council Directives 87/18/EEC on the harmonisation of regulations and administrative provisions relating to the application of the principles of good laboratory practice and the verification of their application for tests in chemical substances f1 and 88/320/EEC on the inspection and verification of good laboratory practice (GLP) f2 .

Annotations

Textual amendments

F1

Substituted by Commission directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use (Text with EEA relevance).

Footnotes

f1

OJ L 15, 17.1.1987, p. 29 .

f2

OJ L 145, 11.6.1988, p. 35 .