The Medicines and Healthcare Products Regulatory Agency adopted 44 recommendations, including a call for AI-enabled devices to be monitored throughout their working life.

The British government will now change up AI-enabled medical device regulation to encourage innovation with the appropriate guardrails.

By Bhanvi Satija LONDON, Oct 6 (Reuters) - AI-based medical devices will need constant monitoring even after they're approved for use, rather than a single pre-approval safety check, the head of the ...

By Heekyong Yang and Hyunjoo Jin SEOUL, Oct 8 (Reuters) - Samsung Electronics on Thursday projected its quarterly profit ...

The global edge AI market is expected to grow from $30 billion in 2026 to $118.7 billion in 2033, demonstrating its effect on ...

With Nvidia's RTX Spark chip and platform, Microsoft's newest laptop is ready to compete with AI heavyweights.

Tools that inform clinical decision-making require rigorous assessments equivalent to processes used to approve drugs and ...

How Indian builders are creating useful hardware and devices that can interface with AI without the need for an app, or ...

Of 1,357 AI devices the FDA has cleared for use in patient care, three were tested on whether patients lived longer or better ...

GigHz highlights a peer-reviewed analysis of 1,430 authorization records and the broader question of what it will take to ...

Compare Plaud NotePin S, SwitchBot AI MindClip, Omi, and Vocci on price, battery, transcription, subscriptions, and the best ...

Microsoft unveiled on Wednesday an AI coding model that can run directly on personal computers and new security technology to ...