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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.
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.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
This procurement policy note is now out of date.
DASA and DE&S are seeking innovative technologies to enable urban-optimised Unmanned Air Systems
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 to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guide contains a description of the technical requirements to be met for consideration of type approval for new mobile preliminary drug-testing devices for police use in Great Britain.
This initiative signals an important step towards a new regulatory framework for medical devices in Great Britain which protects public health, ensures access to MedTech innovations, and maintains an attractive market for industry
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