As healthcare shifts towards remote monitoring, connected devices and decentralized care, sensor technologies are becoming ...

According to Deloitte, only 22% of life sciences leaders say they have successfully scaled AI, and just 9% report achieving ...

Emerging medical-device risks are often missed because early warning signs are fragmented across complaints, manufacturing, ...

The increased digitalization of medical device manufacturing makes lean practices more applicable than ever. Keep these ...

What 524B and QMSR actually require, in plain terms, including the post-market obligation that does not end at clearance? How ...

Catastrophic failures rarely stem from isolated hardware bugs. They breed where hardware, firmware, wireless telemetry, and ...

Post-market surveillance (PMS) systems in the medical device industry have become increasingly sophisticated in collecting complaints, monitoring adverse events, and generating regulatory reports.

MedTech leaders must find a balance between the slow, careful world of medicine and the fast-paced expectations of investors. Real success comes from choosing high-quality science over quick shortcuts ...

Medical device software development teams have always struggled with a deceptively simple question: How much of the system is ...

Infographics can propel MedTech research and campaigns and enhance the user experience. Here Fabricio Pamplona, co-founder of online infographic maker for scientists Mind the Graph, explores the power ...

Market Access is now the central input into M&A and value-driven divestitures, enabling MedTech leaders to reshape portfolios for strategic advantage, long-term growth, and greater value to patients – ...

Artivion has finalized its acquisition of Endospan Ltd., adding the FDA-approved NEXUS Aortic Arch System to its portfolio of aortic arch therapies. The deal strengthens the company’s position in the ...