# The Veterinary Medicines Regulations 2013, Paragraph 3: Manufacture

Extent: E+W+S

(1) The product must have been manufactured by—
(a) the holder of a manufacturing authorisation if manufactured in Great Britain;
(b) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(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) Sub-paragraph (1)(d) does not apply where the United Kingdom has a formal agreement with the exporting country that includes mutual recognition of good manufacturing practice or where the Secretary of State is satisfied that the exporting country requires manufacturers of veterinary medicinal products to apply standards of good manufacturing practice which are at least equivalent to those in Great Britain.

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Source: https://www.legislation.gov.uk/uksi/2013/2033/schedule/6/paragraph/3 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2013/schedule-6/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.