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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
Guidance for manufacturers of cardiac implantable electronic devices and their leads. It outlines specific scenarios that should be considered when determining if an incident is reportable.
How to write clear and effective field safety notices (FSNs) for medical devices.
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