# The Veterinary Medicines Regulations 2013, Paragraph 1: Manufacturing authorisation

Extent: E+W+S

(1) 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”).
(2) For the purposes of sub-paragraph (1) the activities are—
(a) the manufacture of veterinary medicinal products (whether for use in Great Britain or another country);
(b) 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;
(c) the importation of any veterinary medicinal product for use in Great Britain.

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Source: https://www.legislation.gov.uk/uksi/2013/2033/schedule/2/paragraph/1 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2013/schedule-2/paragraph-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.