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

The course helps professionals navigate complex global regulations for medical software. This two-day course covers key topics including SaMD qualification, regulatory positioning, cloud-based ...

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

The list ranks companies according to their annual revenues from medical devices and supply segments (in U.S. dollars). Market caps are for whole companies. Companies that focus on distribution, ...

The industry’s heavy reliance on waterfall project management has resulted in long, siloed, and high-risk product development ...

With close collaboration between sponsors, CROs, and regulators, this emerging technology has the potential to greatly ...

The Food and Drug Administration’s (FDA) recent rejection of all study data from Mid-Link Testing highlights the importance of using reliable, ...

Sequana Medical announced today that CMS recommended that its Alfapump system become eligible for a new incremental payment.

From El Paso, Texas, to Richmond, Virginia, medical device warehouses are leaking ethylene oxide, a cancer-causing chemical.

Eyenovia provides development update on Optejet user filled device: New York Monday, April 14, 2025, 14:00 Hrs [IST] Eyenovia, Inc, an ophthalmic technology company developing and ...

Global pharma major Lupin Limited (Lupin) on Thursday announced that it has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (US FDA), for ...