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Information for manufacturers of medical devices on post-market surveillance, 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.
The Foreign, Commonwealth & Development Office (FCDO) invited UK school students to write about big economic challenges by 29 June 2025. Competition now closed.
Guidance for industry on preparing responses to good laboratory practice (GLP) and good clinical practice (GCP) inspection reports.
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.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
How to write clear and effective field safety notices (FSNs) for medical devices.
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