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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.
Notices of publication and a consolidated list for designated standards for medical devices.
Advice on writing clear notices and maximising replies to your FSNs.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
The Innovative Devices Access Pathway (IDAP) pilot is designed to accelerate the development of innovative medical devices that meet an unmet clinical need in the NHS and support their integration into the UK market.
From today, regulations enforcing consumer protections against hacking and cyber-attacks will take effect, mandating that internet-connected smart devices meet minimum-security standards by law.
Notices of publication and a consolidated list for designated standards for in vitro diagnostic medical devices.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
The CMA is carrying out a market investigation in respect of the supply of mobile browsers and browser engines, and the distribution of cloud gaming services through app stores on mobile devices in the UK.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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.
How to test your service for different browsers and devices: user needs, verified browsers, adapting to change.
The Medicines and Healthcare products Regulatory Agency (MHRA) has designated three new UK Approved Bodies, almost doubling the UK’s capacity to certify medical devices, supporting faster certification of safe and effective medical devices for healthcare professionals and the public.
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