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33.—(1) Where a veterinary medicinal product is authorised using mutual recognition or the decentralised procedure, the Secretary of State is the competent authority for the purposes of Commission Regulation (EC) No 1084/2003 (concerning the examination of variations to the terms of a marketing authorisation for medicinal products for human use and veterinary medicinal products granted by a competent authority of a member State)(1) or, from 1st January 2010, Commission Regulation (EC) No 1234/2008 (concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products)(2).
OJ No L 159, 27.6.2003, p. 1.
OJ No L334, 12.12.2008, P.7.
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