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Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
To offer credit to consumers you must be authorised by the Financial Conduct Authority (FCA) and join the Financial Services Register
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Guidance for manufacturers, their authorised representatives and importers.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Find out about exporting products of animal origin (POAO) such as meat, dairy and fish, live animals, plants and plant products.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
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.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Check the tariff classification for preparations put up for retail sale.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Things to consider when buying and using products.
The way you apply to licence biological products has changed
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