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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information and guidance on a range of medical devices for users and patients.
How to get fast-track approval of medical devices during COVID-19.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Order a certificate of free sale to export medical devices outside the UK.
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.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to conform with the legal requirements for placing medical devices on the market.
Information about the EU Regulations and their implementation in Northern Ireland
It’s illegal to hold a phone or a sat nav while driving - you'll get penalty points, a fine and can be banned from driving.
Information to support commercial fishers on under 12 metre English vessels.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
The MHRA has conducted a thorough assessment of technical and biological safety information provided by NSO and is satisfied that the modified MAGEC X system can now be used in the UK.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Advice on writing clear notices and maximising replies to your FSNs.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
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