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Title III Requirements for specific marketing authorisation applications

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

Notes on Annex II

Footnotes

f1

This Annex will be amended by the Commission in accordance with Articles 146 and 153. All references to Articles or to ‘this Directive’ in this Annex, unless otherwise specified, are to be understood as references to Directive 2001/82/EC.