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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How manufacturers can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
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.
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