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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Submission dates and how the submissions using the EC decision reliance procedure work.
Browse cases data for specific areas within the UK.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How ship security is managed in the UK, and how to comply with UK regulations on ship security.
Sign up for upcoming webinars to learn more about UK transition.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
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