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Information about who could get devices from the Get Help with Technology programme and how devices were allocated to disadvantaged children and young people.
Information about the EU Regulations and their implementation in Northern Ireland
Information and guidance on a range of medical devices for users and patients.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The home page for DSIT’s work supporting the secure and sustainable deployment of connected places technology, also known as smart cities.
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.
Advice on writing clear notices and maximising replies to your FSNs.
Guidance to help you manage the security of your devices and help protect your privacy
How to get fast-track approval of medical devices during COVID-19.
Guidance on choosing evaluation study types and methods.
Checklists providing a practical guide to using medical devices.
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