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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.
Find out about the long-term effects some people can have after having COVID-19.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
Find a BFPO number, send mail to and from British forces personnel and their families
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How the MHRA assesses marketing authorisation applications (MAA) for medicines referred under Article 29.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
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