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Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Requirement to analyse samples from food producing animals for residues of veterinary medicines and prohibited substances.
Change to the information provided on adverse events in the Summary of Product Characteristics for Librela Solution for Injection for Dogs (All strengths)
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.
Benefit-Risk Submission Report (BRSR) and Pharmacovigilance Sales Submission (PSS) templates and guidance for completion of BRSRs, PSSs and signal notifications.
All national applications will be processed on one of six timetables that vary in length depending on the complexity and nature of the application under assessment.
Residues of veterinary medicines in food 2025 surveillance results, a rolling summary.
Panacur C granules seized at East Midlands Airport.
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