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Advice for manufacturers of Class I medical devices for placing products on the UK market
List of Field Safety Notices from 22 to 26 April 2024.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Explains what local authorities should do before publishing their data.
Advice for medical professionals to follow when assessing drivers with diabetes mellitus.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Detention services order 05/2014 about the installation and removal of electronic monitoring devices from detainees.
Advice on writing clear notices and maximising replies to your FSNs.
Use this form (VMS2) to register or re-register your vessel monitoring system device.
Guidance on choosing evaluation study types and methods.
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