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How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
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 for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to apply to protect a spirit drink name under the UK GI schemes.
How to display the legal name for your food product.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
Guidance for suppliers and dealers.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
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