REGISTRATION PROCEDURE FOR VETERINARY MEDICINAL PRODUCTS WITH A CENTRALISED MARKETING AUTHORISATION

Please be informed that the procedure required for submission at the national level for the registration of veterinary medicinal products with a Centralised Marketing Authorisation (MA) issued by the European Medicines Agency (EMA), have been posted on the website of the National Organization for Medicines (EOF) (Path: Veterinary Products / Procedures-Supporting Documentation-Veterinary-Centralised).