The IMDRF have recently published key concepts and principles for the development of high-quality medical devices which ...

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 ...

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

"Prof. Valmed" was the first company to receive approval from the European Union for its co-pilot of the same name.

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

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

Chancellor Professor Colin Stirling, MDRI Director Professor Karen Reynolds, Minister for Trade and Investment Joe Szakacs ...

Rigid and flexible packaging solutions manufacturer Nelipak is investing in the future of sterile barrier medical packaging ...

CMS proposes approval of additional payment for Sequana Medical’s alfapump system in hospital inpatient cases: Ghent, Belgium Tuesday, April 15, 2025, 17:00 Hrs [IST] Sequana Me ...