Work of VMD
The work of VMD is divided into three main areas, or "businesses":
- Licensing – the assessment of applications; issuing and maintenance of Marketing Authorisations; pharmacovigilance for veterinary medicines; and the licensing and inspection of manufacturers and wholesale dealers of veterinary medicines – main customers are Marketing Authorisation holders; manufacturers and importers of veterinary medicines; manufacturers of medicated animal feedingstuffs; retailers of veterinary medicines and medicated animal feedingstuffs; the veterinary profession; farmers and keepers of animals; other stakeholders include the European Medicines Agency (EMEA); DH; Food Standards Agency (FSA); and consumers.
- Residues – the surveillance for residues of veterinary medicines and banned substances in home produced livestock and animal products and imported animal products, reporting of results and co-ordinating follow-up action – we have contracts with other agencies and companies who carry out work on our behalf at abattoirs and other first processing industries, on farms and at retailers of meat and other animal products, and at ports. We also work with other stakeholders including consumer representative groups, the European Commission and the FSA.
- Policy – servicing, developing and implementing new policy/legislation on all aspects of veterinary medicines. Providing support to Ministers through briefing and advice on replies to correspondence and Parliamentary Questions. Day-to-day management of the veterinary medicines (R&D) programme on behalf of the Policy customer (Animal Health and Welfare Directorate, Defra) – we work closely with Ministers and officials of Defra and other Government Departments and Agencies including the FSA, the general public, industry, consumer representative groups, the European Commission, embassies and other representatives of foreign governments.
Read more about this topic: Veterinary Medicines Directorate
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