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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
The CMA is investigating Apple’s conduct in relation to the distribution of apps on iOS and iPadOS devices in the UK, in particular, the terms and conditions governing app developers’ access to Apple’s App Store.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Information about the EU Regulations and their implementation in Northern Ireland
Get help classifying computers, inkjet and toner cartridges and their components.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to conform with the legal requirements for placing medical devices on the market.
How to get fast-track approval of medical devices during COVID-19.
How schools can enrol iPads in Apple School Manager (ASM), set up iPads and make the most out of them.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
Information to support commercial fishers on under 12 metre English vessels.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
Using recommended patterns for workplace wifi networks and sharing infrastructure.
Guidance to assist fishers understand how and when I-VMS will be delivered in English waters, how it may affect them, their responsibilities, and the steps they need to consider.
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