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How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (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.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Information about the EU Regulations and their implementation in Northern Ireland
Information about who could get devices from the Get Help with Technology programme and how devices were allocated to disadvantaged children and young people.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information and guidance on a range of medical devices for users and patients.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Advice on writing clear notices and maximising replies to your FSNs.
Checklists providing a practical guide to using medical devices.
How to get fast-track approval of medical devices during COVID-19.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
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