Professionals enrolled in the certificate will develop an understanding of critical regulatory, economic, and legal issues in addition to the project management skills that facilitate the development ...

A comprehensive and in-depth analysis of US medical device diagnostics development and approval ... premarket approval, 510(k) application process and product development protocol and review process.

Avoid common pitfalls and transform your customer visits into powerful catalysts for user-inspired device design and ...

Comprehensive and in-depth analysis of US medical device diagnostics development and approval ... 510 (k) application process, and product development protocol and review processes.

By Sunil Inamdar, Vice President of Technical Development, Polyzen Specialized, custom-shaped low-pressure balloons are ...

Discover how AI, cybersecurity, and smart factory innovations are revolutionizing medical device manufacturing.

The 3rd Medical Device Software Development Summit returns to Munich in January! The European market is capturing 30% of the global medical device field driven by rapid advances in innovative ...

EOS GmbH, headquartered in Krailling, Germany, has announced its latest advancement in regulatory compliance support for ...

A subset of PFAS made possible the development of medical ... chemical alternatives, but the process is lengthy and complicated. Many medical devices must be approved by the FDA, and replacement ...