Medical device makers must balance PFAS performance benefits with health risks, preparing for regulation by auditing ...

The question is not whether AI will transform healthcare; it’s whether regulators can keep pace with that transformation.

The rise of AI in health care presents new challenges related to the patentability and regulation of AI-driven medical ...

Short Summary The EU, UK, and USA each have distinct and evolving regulatory systems for medicines and medical devices, involving strict approval, surveillance, and market access requirements managed ...

Regulation of artificial intelligence (AI) in Asia Pacific remains nascent, mostly governed by existing regulatory frameworks designed for ...

The company said the FDA’s nod validates its proprietary system as a "potentially unique solution for the large, underserved ...

Zacks Medical Info Systems industry stocks like VEEV, HIMS and BFLY are expected to gain from the Stargate Project and ...

COIMBATORE: The state government is set to establish the first Medical Devices Testing Laboratory in Coimbatore district for ...