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Requirements for Marketing Authorisation applications for particular veterinary medicinal products.
Legal requirements referred to Article 8(1), Point (B) of the Veterinary Medicines Regulations, as amended.
Requirements for Specific Marketing Authorisation Applications.
Requirements for Immunological Veterinary Medicinal Products.
The documentation accompanying an application for a marketing authorisation pursuant to Schedule 1 of the Veterinary Medicines Regulations shall be presented in accordance with the requirements set out in this Annex.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
How to complete and submit the turnover declaration form as the holder of a UK marketing authorisation.
Fees charged for the specific activities carried out by the VMD.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
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.
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.
Fixed term appointment vacancies in the Residues Team.
Reporting against VMD published standards up to 31 March 2025.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Marketing Authorisations Information Service (MAVIS) Hub edition 130
New legislation in Great Britain will make changes to the requirements set out in the Veterinary Medicines Regulations 2013.
Unauthorised product from the USA seized at a Portadown courier company.
Information and resources on the UK’s plans to see antimicrobial resistance contained and controlled by 2040.
Senior Efficacy Assessor vacancies, working in the regulation of veterinary medicines.
Panacur C granules seized at East Midlands Airport.
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