Increase in suspected adverse event reports following use of Caninsulin 40 IU/ml Suspension for Injection.
Veterinary Medicines Directorate
- Peer Reviewer contracts extended
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- GCA Annual Conference 2024?
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Residues of veterinary medicines in food 2024 surveillance results, a rolling summary.
How to contact the VMD for specific services or enquiries.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 April to 30 June 2024.
Biological Assessor vacancy, working on applications for veterinary medicinal products.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Product defect recall alert for: Fleasolve 134 mg Spot-on Solution for Medium Dogs Vm 49507/4004 by Naqua Ltd.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Head of Information Technology vacancy to lead teams to deliver a wide range of IT services that support internal and external stakeholders.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
The post-holder will be part of the VMD’s Supply Team within our Regulatory Affairs Section in the Authorisation Division.
Changes to our special imports digital service will affect UK veterinary surgeons and WDA holders who hold and supply imported medicines.
Changes to our special imports digital service will affect UK veterinary surgeons and WDA holders who hold and supply imported medicines.
Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.
Change to the information provided on adverse events in the Summary of Product Characteristics for Neptra Ear Drops Solution for Dogs.
Change to the information provided on adverse events in the Summary of Product Characteristics for Neptra Ear Drops Solution for Dogs.
Results of our 2024 pharmaceutical industry customer survey carried out by an independent party.
International Office vacancy, working on international projects for the VMD.
Non-UK authorised medicine seized at East Midlands Airport.
Non-UK medicine seized at East Midlands Airport.
Change to the information provided on adverse events in the Summary of Product Characteristics for Cimalgex 8 mg / 30 mg / 80 mg Chewable Tablets for Dogs.
Change to the information provided on adverse events in the Summary of Product Characteristics for Propalin Syrup, 40 mg/ml Dogs.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Recall alert for Johnson’s 4Fleas 11.4 mg Tablets for Cats and Kittens 6-tablet pack for incorrect packaging relating to 4Fleas Tablets for Dogs 6-tablet pack.
Veterinary products seized during an FDA (US Food and Drug Administration) Operation.
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.
Fees charged for the specific activities carried out by the VMD.
VICH consultation until 30 November 2024 on guidelines relating to the technical requirements for demonstrating genotoxic safety of residues of veterinary drugs in human food.
Reporting against VMD published standards up to 31 March 2025.
Dermipred tablets seized at East Midlands Airport.
Biheldon cat and dog wormers seized at East Midlands Airport.
Pharmaceutical Assessor vacancy, working in the regulation of veterinary medicines.
Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.
Explainer for the pharmaceutical industry on the implementation of Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.
Adored Beast products stopped at East Midlands Airport.
GIGI Vet supplements stopped at East Midlands Airport.
Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a shared-label for use on veterinary medicines placed on the market in the UK and Ireland.
This is the Hub for all the Veterinary Medicines Directorate's communications on current and future regulatory changes.
Once a VMP is on the UK market an MAH must record and submit the results of their signal management process, alongside sales and worldwide authorisation status data.
Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
New legislation in force from today in Great Britain makes changes to the requirements set out in the Veterinary Medicines Regulations 2013.
Records that must be kept when supplying or administering veterinary medicines in the UK.
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