The Veterinary Medicines Directorate (VMD) is an Executive Agency of the Department for Environment, Food and Rural Affairs

Department for Environment, Food and Rural Affairs

The Department for Environment, Food and Rural Affairs is the government department responsible for environmental protection, food production and standards, agriculture, fisheries and rural communities in the United Kingdom...

 (Defra) seeking to protect public health, animal health, the environment and promoting animal welfare by assuring the safety, quality and efficacy of veterinary medicines in the United Kingdom

United Kingdom

The United Kingdom of Great Britain and Northern IrelandIn the United Kingdom and Dependencies, other languages have been officially recognised as legitimate autochthonous languages under the European Charter for Regional or Minority Languages...

.

Responsibilities

The VMD is responsible for:

• the assessment, issue and maintenance of all national Marketing Authorisations for veterinary medicines in accordance with European Community and UK
  United Kingdom
  The United Kingdom of Great Britain and Northern IrelandIn the United Kingdom and Dependencies, other languages have been officially recognised as legitimate autochthonous languages under the European Charter for Regional or Minority Languages...
  
   legislation;
• acting as rapporteur/co-rapporteur or reference member state/concerned member state for designated European applications for centralised or decentralised authorisations;
• controls on the manufacture and distribution of veterinary medicinal products including inspections;
• pharmacovigilance
  Pharmacovigilance
  Pharmacovigilance is the pharmacological science relating to the detection, assessment, understanding and prevention of adverse effects, particularly long term and short term side effects of medicines...
  
   through the surveillance of suspected adverse reactions (SARs), through the Suspected Adverse Reaction Surveillance Scheme
  Suspected Adverse Reaction Surveillance Scheme
  This article is about Veterinary Medicines. For Human Medicines, see the Yellow Card Scheme.The Suspect Adverse Reaction Surveillance Scheme used by the Veterinary Medicines Directorate is similar to the Human Yellow Card Scheme...
  
   (SARSS) - veterinary surgeons fill in form VLM252A;
• surveillance for residues of veterinary medicines in animals and animal products;
• the provision and implementation of policy advice on these matters to the Health and Agriculture Ministers who jointly form the Licensing Authority for veterinary medicines under the Medicines Act 1968;
• the management of the Research & Development (R&D) programme linked to veterinary medicine issues; and
• the co-ordination of Defra’s work in the area of antimicrobial resistance via the DARC Group, including development of a Government Veterinary Antimicrobial Resistance Surveillance Strategy.

History

VMD was first established in 1989 and from 1990 was a Next Steps Agency of the Ministry of Agriculture, Fisheries and Food (MAFF)

Ministry of Agriculture, Fisheries and Food

The Ministry of Agriculture, Fisheries and Food was a United Kingdom government department created by the Board of Agriculture Act 1889 and at that time called the Board of Agriculture, and then from 1903 the Board of Agriculture and Fisheries, and from 1919 the Ministry of Agriculture and Fisheries...

. It became an Executive Agency of Defra on 7 June 2001.

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)
  European Medicines Agency
  The European Medicines Agency is a European agency for the evaluation of medicinal products. From 1995 to 2004, the European Medicines Agency was known as European Agency for the Evaluation of Medicinal Products.Roughly parallel to the U.S...
  
  ; DH; Food Standards Agency (FSA)
  Food Standards Agency
  The Food Standards Agency is a non-ministerial government department of the Government of the United Kingdom. It is responsible for protecting public health in relation to food throughout the United Kingdom and is led by a board appointed to act in the public interest...
  
  ; 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.

Costs

Operational costs are recovered through charges to the veterinary pharmaceutical industry, the food industry, and Defra.

During 2003/2004 operational costs totalled £11,960,000:

• Licensing: £4,915,000 (paid for by the veterinary pharmaceutical industry)
• Statutory Residues: £3,693,000 (paid for by the food industry)
• Non-statutory Residues: £1,054,000 (paid for by Defra)
• Policy: £2,298,000 (paid for by Defra)

External links

VMD website