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Explainer for businesses and persons regulated by the Veterinary Medicines Regulations 2013, as amended, on the transitional provisions included in the amending legislation: the Veterinary Medicines (Amendment etc.) Regulati…
Registers of authorised manufacturers, wholesale dealer sites and retailers.
How to obtain an authorisation to wholesale veterinary medicines.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance for Marketing Authorisation Holders and holders of other types of authorisations on their responsibilities for veterinary pharmacovigilance and how to report suspected Adverse Events.
Marketing Authorisations Information Service (MAVIS) Hub edition 130
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
This enforcement policy sets out the general principles and approach taken by the VMD.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance for the veterinary pharmaceutical industry on applying for maximum residue limits (MRLs) in the UK.
How veterinary medicines can be advertised.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
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.
Effective from 17 May 2024 Definitive fees charged for applications under Schedule 7 of Veterinary Medicines Regulations 2013 (as amended) as they apply to GB.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
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.
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