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Residues of veterinary medicines in food 2020 surveillance results.
Marketing Authorisation Holders (MAHs) have informed the VMD of supply problems with the following lactating cow intramammary antibiotics.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Reporting against VMD published standards up to 31 March 2021
This is the Hub for all the Veterinary Medicines Directorate's communications on current and future regulatory changes.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Explainer for marketing authorisation holders, manufacturers, wholesale dealers, retailers (including veterinary surgeons) and feed business operators on the manufacture and movement of veterinary medicines.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Marketing Authorisations Information Service (MAVIS) Hub edition 117
Product defect recall alert for: Otodex Skin Cream (Vm 13240/4000) by Petlife International Ltd
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Freedom of Information (FOI) requests received by the Veterinary Medicines Directorate (VMD) 1 July and 31 December 2019.
For a marketing authorisation holder only; how to report a defect with a veterinary medicine.
Guidance for Marketing Authorisation Holders and holders of other types of authorisations on their responsibilities for veterinary pharmacovigilance and how to report suspected Adverse Events.
UK-Canada Regulatory Cooperation: Guidance on Veterinary Drug Simultaneous Reviews published.
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