KFDA sets global standard for generative AI medical device approval guidelines Health authority introduces pioneering ...

The growing internet of medical things (IoMT) has unique definitions and testing requirements.

The millions of people residing in urban, semi-urban, rural, and remote areas, the lack of adequate healthcare infrastructure ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

Europe medical device market was valued at $144.4 billion in 2022 and will grow by 4.7% annually over 2022-2032, driven by the prevalence of infectious diseases as well as the increasing prevalence of ...

Global medical device market will reach $882.3 billion by 2032, growing by 5.5% annually over 2022-2032 owing to aging population worldwide, the prevalence of infectious diseases as well as the ...

When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...

A cutting-edge medical device which purifies and concentrates urine could be game-changing in the research and diagnosis of ...

Ageing patient populations and technological advancements are emerging as key drivers of healthcare innovation and delivery.

Abbott Laboratories (NYSE: ABT) is a well-diversified health care company, with four distinct units: medical devices, ...

The point is that we generally consider light to be good, safe, even comforting. Yet when it comes to our skin, things are a ...