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How a marketing authorisation holder should report a defect with a veterinary medicine.
Things to consider when buying and using products.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Check what you need to do to sell cosmetic products in Great Britain.
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.
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
The way you apply to licence biological products has changed
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
How to create a model of how your digital health product works and choose measures for your evaluation.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
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.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Compare different evaluation approaches and choose an appropriate method.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in 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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