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Bring photo ID to vote Check what photo ID you'll need to vote in person in the General Election on 4 July.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Guidance to help you manage the security of your devices and help protect your privacy
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.
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
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.
The Devices Expert Advisory Committee (DEAC) replaces the Committee on Safety of Devices and is responsible for providing independent, external expert input and advice on a wide range of aspects relating to medical devices to help the Medicines and Healthcare...
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (21 May 2024) launched a four-week consultation which will support improved safety for certain high risk in vitro diagnostic (IVD) devices.
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
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