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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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 for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
This project offers the first rigorous assessment of the role of information and subsidies in public transport safety choice
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Advice on writing clear notices and maximising replies to your FSNs.
Information and guidance on a range of medical devices for users and patients.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
Guidance on managing and using bed rails safely.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
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