The success in intra-European healthcare deals requires regulatory expertise, operational flexibility and market-specific ...

Medtech: Medical technology Medical Device Regulation: The European Union’s Medical Device Regulation is commonly abbreviated as MDR. Medical Device Reporting: MDR is one of the FDA’s tools to monitor ...

Medtech giant Edwards Lifesciences made a move in the sector when it bought Israeli mitral valve device specialist Innovalve Bio Medical for $300m. However, the rise in prevalence of heart disease ...

Remote medtech jobs can seem hard to come by compared to tech firms that work more with software. But there are medical device companies — including developers, manufacturers and medtech industry ...

Infusion pumps, glucose monitors, insulin pumps and dental implants were among the products with delayed side effect reporting TUESDAY, March 18, 2025 (HealthDay News) -- Other people could be ...

That’s because medical device manufacturers frequently fail to promptly report side effects caused by their wares to federal regulators, a new study says. About 3 in 10 adverse event reports for ...

That’s because medical device manufacturers frequently fail to promptly report side effects caused by their wares to federal regulators, a new study says. About 3 in 10 adverse event reports for ...

the Company's compliance with medical device reporting regulations to report adverse events involving the Company's products, which could result in voluntary corrective actions or enforcement ...

WALTHAM, Mass., March 13, 2025--(BUSINESS WIRE)--Paragonix Technologies, a pioneer in organ transplant technologies and organ procurement services, announced today that five of its devices have ...

Medical Device Regulation 2017/745, commonly referred to as EU MDR. This approval further confirms Paragonix’s compliance with the highest quality control standards for medical devices and ...