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Division TITLE II REQUIREMENTS FOR IMMUNOLOGICAL VETERINARY MEDICINAL PRODUCTSF1

United Kingdom

Original text. Later amendments are not shown.

Without prejudice to specific requirements laid down by Community legislation for the control and eradication of specific infectious animal diseases, the following requirements shall apply to immunological veterinary medicinal products, except when the products are intended for use in some species or with specific indications as defined in Title III and in relevant guidelines.

  1. PART 1:SUMMARY OF THE DOSSIER
  2. PART 2:CHEMICAL, PHARMACEUTICAL AND BIOLOGICAL/MICROBIOLOGICAL INFORMATION (QUALITY)
  3. PART 3:SAFETY TESTS
  4. PART 4:EFFICACY TESTS
  5. PART 5:PARTICULARS AND DOCUMENTS
  6. PART 6:BIBLIOGRAPHICAL REFERENCES

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).