# The Veterinary Medicines Regulations 2013, Paragraph 1


In this Schedule—
“converted EU marketing authorisation” means an EU marketing authorisation to which paragraph 2 applies;
“EU marketing authorisation” means a marketing authorisation for a veterinary medicinal product granted by the European Commission in accordance with Title 3 of Regulation (EC) No 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.

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