Paragraph 1 Manufacturing authorisationF1E1
England, Wales and Scotland
No person may carry out any activity mentioned in sub-paragraph (2) otherwise than in accordance with an authorisation granted under this Schedule (a “manufacturing authorisation”).
For the purposes of sub-paragraph (1) the activities are—
the manufacture of veterinary medicinal products (whether for use in Great Britain or another country);
the carrying out of any part of the manufacturing process or of bringing a veterinary medicinal product to its final state, including the processing, assembling, packaging or repackaging, labelling or relabelling, storing, sterilising or releasing for supply of a veterinary medicinal product;
the importation of any veterinary medicinal product for use in Great Britain.
Annotations
Textual amendments
- F1
Sch. 2 para. 1 substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 80
Extent
- E1
This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only