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Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 April to 30 June 2025.
Information for farmers about inspections carried out on farms using on-site feed mixers to add veterinary medicines into feed.
Apply for authorisation of premises for the retail supply of POM-VPS and NFA-VPS veterinary medicines by suitably qualified persons (SQPs).
Requirements for handling complaints, returns, suspected counterfeits and recalls.
Fees are charged for new marketing authorisation (MA) applications and variations to MAs.
Guidance for vets, farmers and animal keepers on what the mg/PCU means and how it is calculated.
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…
The following requirements shall apply to immunological veterinary medicinal products, except where otherwise set out in Section IV.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Summary of product characteristics for BLUEVAC-3 BTV-3 vaccine in the UK
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a shared-label for use on veterinary medicines placed on the market in the UK and Ireland.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 April to 30 June 2024.
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.
The following detailed requirements shall apply to veterinary medicinal products other than biological veterinary medicinal products, except where otherwise set out in Section IV.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to 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.
Criteria applied by the VMD for accepting and agreeing the invented name of veterinary medicinal products.
Details of the VMD Corporate Priorities for 2025 - 2026.
These published standards relate to Corporate Priority 3 – Regulatory Service.
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