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References and list of enforcement notices and prosecutions which involved illegal activity with animal medicines in the last year.
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Service for Marketing Authorisation Holders.
Records that must be kept when supplying or administering veterinary medicines in the UK.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
The Veterinary Medicines Regulations require wholesale dealers in Great Britain to adhere to Good Distribution Practice for all distribution processes.
Benefit-Risk Submission Report (BRSR) and Pharmacovigilance Sales Submission (PSS) templates and guidance for completion of BRSRs, PSSs and signal notifications.
List of words and phrases that will cause a veterinary product to be medicinal by presentation either through use or contextual use.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Action following notification of suspension or expiry of an authorisation to market an animal medicine if it fails to comply with the regulations.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
How authorised veterinary medicines, products supplied under the cascade and products used under the Veterinary Medicines Internal Market Scheme and Veterinary Medicines Health Situation Scheme can be advertised.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
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 Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.
How to obtain an authorisation to wholesale veterinary medicines.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives in Great Britain and Northern Ireland.
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