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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to apply for a regulatory advice meeting on medical devices and in vitro diagnostic devices.
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
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.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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