APPLICATIONS PAGE

In order for a veterinary medical product to be placed on the market in the UK an authorisation from the VMD is required. There are many types of authorisation to meet different circumstances that can be applied for through the VMD which is the licensing authority for the United Kingdom

The main UK guidance on legislation, when submitting an application can be found in a series of leaflets - the Veterinary Medicines Guidance Notes (VMGN). These explain how and what to do when you need to submit an application. These guidance notes are designed to assist our customers to interpret and apply both UK and EC legislation on veterinary medicines.

Details of the Veterinary Medicines Regulations can be found here

Lists of authorised products with their Summary of Product CharacteristicsDetails and details of our work, plans and results can be found in the VMD's quarterly publication The Marketing Authorisations Veterinary Information Service (MAVIS).  It also contains short information paragraphs about overall developments on the controls of veterinary medicines. Some contact names and numbers can also be found in MAVIS.

Should you require a copy of any of the application forms, they can be downloaded from this site. They will either be in Microsoft Word format (.doc) or Adobe Reader Format (.pdf).

 

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