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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.
Product Safety Report for Step Down Transformer presenting a serious risk of electric shock.
The Medicines and Healthcare products Regulatory Agency (MHRA) have embarked upon an ambitious programme of reform to ensure that medical device regulation is fit for purpose for software, including artificial intelligence (AI).
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.
Information and guidance on a range of medical devices for users and patients.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Cabinet Office Minister Baroness Neville-Rolfe spoke at techUK about new data and technology innovations that could transform the UK border
What the retirement of analogue phone lines, also known as the Public Switched Telephone Network (PSTN), means for you.
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.
Order a certificate of free sale to export medical devices outside the UK.
Information for manufacturers, healthcare organisations and professionals, researchers, and patients & public on Software as a Medical Device (SaMD), including Artificial Intelligence as a Medical Device (AIaMD).
Statistics on the Police use of TASER ® X26 conducted energy devices across England and Wales.
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