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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.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Getting a UK background check so you can apply for Global Entry and get through USA border control faster: how to apply, how much it costs
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information about moving to, living or retiring in the USA – including visas, working, healthcare and driving.
How to conform with the legal requirements for placing medical devices on the market.
How to link charities to make accounting and reporting easier.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Data First is a pioneering data-linking, research and academic engagement programme led by the Ministry of Justice and funded by ADR UK.
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