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Recent Posts
Is your company prepared for the new EU MDR? Michael Santalucia, Vice President of Global Regulatory Affairs for Terumo...
The global life sciences market is witnessing an unprecedented pace of change across pharmaceuticals, medical devices,...
This October, Mark Wehde, Section Head of Technology Development at the Mayo Clinic Division of Engineering, will join...
Quality management is an integral factor in the development, approval, and commercialization of medical devices. With...
Prior to joining Fresenius, Norbert worked as a Program Manager at other medical device companies in the San Francisco...
In the lead-up to the American Medical Device Summit, we are highlighting some of the incredible women of the medical...
While the American medtech industry is thriving, it still must deal with challenges that include higher production...
In a recent study conducted for Pilgrim, quality and compliance professionals from the top 2,000 Pharmaceutical,...
Recognizing that their traditional approach to moderate and higher-risk, hardware-based medical devices is not well...
One of the promises of additive manufacturing is the ability to go after niche markets with low volume production of...