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Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
How to obtain an authorisation to wholesale veterinary medicines.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
References and list of enforcement notices and prosecutions which involved illegal activity with animal medicines in the last year.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
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.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
A quality system is required to ensure that the objectives of good distribution practice are realised and should clearly set out responsibilities, processes and risk management principles in relation to the wholesale dealers鈥�
Principles of good distribution practice for veterinary medicinal products.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
How to report suspected illegal activity and how we will deal with these reports.
Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
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