Paragraph 1 F1

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.