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Data, Freedom of Information releases and corporate reports
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
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.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
What you need to do if you sell or store tobacco products in the UK.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to create a model of how your digital health product works and choose measures for your evaluation.
Guidance for suppliers and dealers.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
You must get permission to export certain drugs and medicines.
How to write up and share your findings
Guidance for EU exporters from 31 January 2024, exporters from rest of the world from 30 April 2024 and UK importers, on how to import groupage or mixed load consignments of animal products into Great Britain (England, Scotland and Wales).
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to use the Trade Tariff tool or get help to classify your goods, so you pay the right amount of Customs Duty and import VAT.
What you need to do if you manufacture or import tobacco products in the UK.
Guidance for businesses on EU Regulation 2019/1020 on Market Surveillance and Compliance of Products.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
The documents you need and the border checks your import must pass to import from non-EU countries.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
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