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Clarification for the interpretation of the new elements within the Veterinary Medicines Regulations (VMRs), as amended, relating to combating antimicrobial resistance (AMR).
Information about who will inspect your farm or land, what they’re looking for and any penalties you may get.
Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
Change to the information provided on adverse events in the SPC for Apoquel Film-coated Tablets for Dogs and Apoquel Chewable Tablets for Dogs.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
The main decision-making, executive and managerial bodies at the Veterinary Medicines Directorate (VMD).
This UK VARSS report provides the details of UK veterinary antibiotic resistance and sales surveillance.
Anyone can report an illegal medicine or prescription misuse and a company can use these forms to report a supply problem or product defect.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
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.
The documentation accompanying an application for a marketing authorisation pursuant to Schedule 1 of the Veterinary Medicines Regulations shall be presented in accordance with the requirements set out in this Annex.
How the Veterinary Medicines Directorate treats your personal information and how to check what details are held on file.
Guidance for vets, farmers and animal keepers on what the mg/PCU means and how it is calculated.
Guidance developed for vets following changes to RCVS guidance on prescribing POM-V medicines.
Ectoparasiticide veterinary medicinal products and reporting adverse events.
Bravecto Chewable Tablets for Dogs seized at East Midlands Airport.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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