# The Veterinary Medicines Regulations 2006, Paragraph 3: Manufacture

Extent: E+W+S+N.I.

(1) The product must have been manufactured by—
(a) the holder of a manufacturing authorisation if manufactured in the United Kingdom;
(b) the holder of a manufacturing authorisation issued under Directive (EC) No. 2001/82 if manufactured in another member State;
(c) in the case of Australia, Canada, New Zealand, or Switzerland, the holder of an authorisation from the competent authority permitting him to manufacture medicinal products;
(d) in the case of any other country, a manufacturer whose premises have been inspected and approved by an officer of the Secretary of State.
(2) This paragraph does not apply until 1st November 2007.

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Source: https://www.legislation.gov.uk/uksi/2006/2407/schedule/6/paragraph/3 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2006/schedule-6/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.