Obligations of the Manufacturer/Importer of Veterinary Medicinal Products

The manufacturer/importer must adhere to the principles and guidelines of Good Manufacturing Practice (GMP) for Veterinary Medicinal Products set out in Cabinet Regulation No. 319 of 15 May 2007 Regulations Regarding the Manufacture and Control of Veterinary Medicinal Products, the Procedure for the Issuance of a Good Manufacturing Practice Certificate to a Manufacturer of Veterinary Medicinal Products and Regarding the Requirements for the Qualification and Professional Experience of the Official Responsible for the Manufacture of Veterinary Medicinal Products and the guidelines of the European Commission, which are published in Volume 4 of the Rules Governing Medicinal Products in the European Union.