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Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
This enforcement policy sets out the general principles and approach taken by the VMD.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Summary of product characteristics for Bultavo-3 BTV-3 vaccine in the UK
Legal requirements referred to in Schedule 1 of the Veterinary Medicines Regulations, as amended.
Legal requirements for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
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.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Advice from the UK Chief Veterinary Officer to veterinarians prescribing BTV-3 vaccines.
Information on vaccination schedules and licensed vaccines for dogs.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Apply for authorisation of premises for the retail supply of POM-VPS and NFA-VPS veterinary medicines by suitably qualified persons (SQPs).
Guidance on the Batch Release Request scheme for an immunological veterinary medicine to be placed on the UK market.
The VMR sets out the statutory fees associated with various regulatory services provided by the VMD. The statutory fees and fee structure are implemented from 17 May 2024.
Guidelines and guidance for vets, farmers and animal keepers on the responsible use of antimicrobials.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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