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 Indian medical device industry faces challenges from international trade dynamics, regulatory barriers, and domestic ...

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 ...

Diagnos Inc. (“DIAGNOS” or the “Corporation”) (TSX Venture: ADK, OTCQB: DGNOF, FWB: 4D4A), a pioneer in early detection of ...

A complete guide to lease accounting for healthcare organizations Making a successful transition to the latest lease accounting requirements such as ASC 842, IFRS 16 or GASB 87 can be a complicated ...

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