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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.
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.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to get access to MHRA submissions portals, how to use them, where to go for help.
How internet scams work and what to be aware of - misleading websites, report website fraud, suspicious communication and phishing, HMRC scams, immigration scams.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
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