Way back in 2001, MD+DI published an article detailing what the author considered to be The Seven Deadly Sins of Medical Device Development. The author reviewed dozens of device development programs ...

The advent of artificial intelligence (AI) and data-driven methodologies has triggered a wave of transformation in regulatory compliance and quality assurance for the development of medical devices.

VOLTAS announces that clean room space within its new facility is now available for medical device startups to rent for ...

I clearly remember standing in the operating room (OR). I was there with our sales representative to observe a case as part of our normal Voice of Customer (VOC) process. I had seen well over 50 ...

Learn how CDMO partnerships can help medtech engineers streamline development and ensure manufacturing excellence.

This online certificate program at Purdue University focuses on regulatory affairs science for medical devices. It equips professionals with knowledge in regulatory processes, quality systems and ...

Hands-on research and applied technology experiences prepare University of New Haven students for careers in high-demand innovation sectors. The University of New Haven has entered into a master ...

Discover how software developers for medical-device OEMs are balancing innovation and safety, and the challenges they face in making it happen. The medical-device industry is rapidly advancing, from ...

The "Playbook for Threat Modeling Medical Devices" was commissioned by the FDA and co-developed by MITRE and MDIC. The Food and Drug Administration on Tuesday announced the release of a new playbook ...

Fueled by convenience, fashion, size and technical innovation, medical devices have evolved from clinical settings to daily consumer use. Today’s highly personalized devices are being embedded into ...