OpenLegislation

Division TITLE III REQUIREMENTS FOR SPECIFIC MARKETING AUTHORISATION APPLICATIONSF1

United Kingdom

Original text. Later amendments are not shown.

  1. 1Generic veterinary medicinal products
  2. 2Similar biological veterinary medicinal products
  3. 3Well-established veterinary use
  4. 4Combination veterinary medicinal products
  5. 5Informed consent applications
  6. 6Documentation for applications in exceptional circumstances
  7. 7Mixed marketing authorisation applications

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).