OpenLegislation

Division TITLE IV REQUIREMENTS FOR MARKETING AUTHORISATION APPLICATIONS FOR PARTICULAR VETERINARY MEDICINAL PRODUCTSF1

United Kingdom

Original text. Later amendments are not shown.

This part lays down specific requirements for identified veterinary medicinal products related to the nature of the active substances contained therein.

  1. 1IMMUNOLOGICAL VETERINARY MEDICINAL PRODUCTS
  2. 2HOMEOPATHIC VETERINARY MEDICINAL PRODUCTS

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).