OpenLegislation

Division 4 F1

United Kingdom

Original text. Later amendments are not shown.

The manufacturing process shall comply with the requirements of Commission Directive 91/412/EEC f1 laying down the principles and guidelines for veterinary medicinal products and with the principles and guidelines on Good Manufacturing Practice (GMP), published by the Commission in The rules governing medicinal products in the European Union , Volume 4.

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 228, 17.8.1991, p. 70 .