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 ...

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

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

The existing online application system has been upgraded with a new auto-generated workflow, and companies are now required ...

Imricor receives CE Mark certification for the Advantage-MR system under new European Medical Device Regulation as it hits ...

Dublin, April 16, 2025 (GLOBE NEWSWIRE) -- The "Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Training Course" has been added to ...

Imricor receives CE Mark certification for the Advantage-MR system under new European Medical Device Regulation as it hits world first with start of VISABL-VT trial. Don't miss out on the ...

Imricor receives CE Mark certification for the Advantage-MR system under new European Medical Device Regulation Approval follows CE Mark certification for the second-generation Vision-MR Ablation ...