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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Learn how to check if your website or mobile app is accessible.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Emergency alerts are broadcast from mobile phone masts. Find out if your phone or tablet can receive alerts.
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