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Explanation of what Pharmacovigilance means and who is responsible. 皇冠体育appse documents must be read with the Implementation Explainer at VMD Information Hub.
Requirement to analyse samples from food producing animals for residues of veterinary medicines and prohibited substances.
Monthly reporting against service standards for answering general enquiries.
Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Check if an online retailer that sells pet medicines is on the Veterinary Medicines Directorate鈥檚 accredited internet retailer scheme (AIRS)
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
How to report suspected illegal activity and how we will deal with these reports.
This UK VARSS report provides the details of UK veterinary antibiotic resistance and sales surveillance.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
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