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Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Register as a manufacturer, importer or distributor of active substances.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
How the MHRA makes decisions on what is a medicinal product (borderline products).
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
How investigators and sponsors should manage clinical trials during COVID-19
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
Proven reoffending quarterly statistics
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information for companies on the import and export of controlled drugs to and from the UK.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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