OpenLegislation

Division INTRODUCTION AND GENERAL PRINCIPLESF1

United Kingdom

Original text. Later amendments are not shown.

This Annex is divided in four titles:

  • Title I describes the standardised requirements for applications for veterinary medicinal products other than immunological veterinary medicinal products.

  • Title II describes the standardised requirements for applications for immunological veterinary medicinal products.

  • Title III describes specific types of marketing authorisation dossiers and requirements.

  • Title IV describes the dossier requirements for particular types of veterinary medicinal products.

  1. 1Division 1
  2. 2Division 2
  3. 3Division 3
  4. 4Division 4
  5. 5Division 5
  6. 6Division 6
  7. 7Division 7
  8. 8Division 8
  9. 9Division 9
  10. 10Division 10

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).