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How to create a model of how your digital health product works and choose measures for your evaluation.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
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.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Use these general provisions to help you determine the origin of your products.
The UK’s consumer connectable product security regime came into effect on 29 April 2024. Businesses in the supply chains of these products now need to be compliant with the legislation.
How to apply for UK protection of a traditional term for a wine product and get it added to the UK traditional terms register.
Things to consider when buying and using products.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Papers from the Office for Product Safety and Standards.
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