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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.
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
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Information about the EU Regulations and their implementation in Northern Ireland
A policy review of the CTDA process, established in July 2021, which governs the validation of antigen and molecular coronavirus (COVID-19) detection tests.
Employment Tribunal decision.
Millions invested in eight innovative companies behind lifesaving new medical technology which could destroy liver cancer tumours, detect Alzheimer’s and quickly spot those at risk of stroke
How we buy goods and services, and how you can work with us.
Home Office approved drug-testing devices.
How to conform with the legal requirements for placing medical devices on the market.
Advice for manufacturers of Class I medical devices for placing products on the UK market
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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