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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Find out about the VAT place of supply rules if your business sells digital services to private consumers.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
A research paper from the CMA
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
A keynote speech by Martin Coleman, Non-Executive Director and Panel Chair of the Competition and Markets Authority (CMA), to the Swedish Competition Authority’s Pros and Cons Conference.
How to renew marketing authorisations for products granted through different routes and at different times.
The British Hallmarking Council's HALO award 2023 is open for submissions.
Pharmacovigilance system requirements
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
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