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Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information and guidance on a range of medical devices for users and patients.
Information about the EU Regulations and their implementation in Northern Ireland
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance to help you manage the security of your devices and help protect your privacy
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to get fast-track approval of medical devices during COVID-19.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to conform with the legal requirements for placing medical devices on the market.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
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