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This page details the government's work to improve the cyber security of enterprise connected devices (or 'IoT' devices.)
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
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 register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
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