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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Blogs where government organisations talk about their work and share information and ideas.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
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