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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.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
FCDO travel advice for Cuba. Includes safety and security, insurance, entry requirements and legal differences.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Resources for individuals and organisations to use supporting a variety of safety awareness campaigns.
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