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Data, Freedom of Information releases and corporate reports
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Advice on writing clear notices and maximising replies to your FSNs.
Management of British armed forces casualties and compassionate cases 24 hours a day, 7 days a week, 365 days a year.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Your rights and security searches, body scans and privacy rules if you're disabled or taking medication aboard aircraft
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
To help our investigations report all HMCTS-related suspicious phone calls, emails, and text messages.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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.
Resources to support exams officers in their important role, covering GCSE, A level, T Level and vocational and technical qualification (VTQ) assessments
Thousands of counterfeit or unbranded copies of LifeVac anti-choking devices are being sold across the UK. The public is reminded to check their product carefully against the images in MHRA guidance to identify whether it is a counterfeit.
Information about the EU Regulations and their implementation in Northern Ireland
Information and guidance on a range of medical devices for users and patients.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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