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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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
How to get access to MHRA submissions portals, how to use them, where to go for help.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
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