Many medical device companies develop software using a traditional waterfall methodology in which each step is taken in sequence: requirements, design, implementation, verification, and validation ...

The Atomic Spectroscopy Group at the National Institute of Standards and Technology, which provides definitive measurements integral to developing biomedical instrumentation that helps diagnose health ...

Engineers could avoid expensive redesigns by planning medical device testing early in development with expert guidance.

WEST CHESTER, Pa.--(BUSINESS WIRE)--Archimedic, a medical device development firm that provides Design, Regulatory, and Go-to-Market services to its clients, has launched OpenQMS, an open-access, ...

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.

Genesis Innovation Group, a medical device development firm, has formed Capitan Orthopedics, a new subsidiary branch, ...

The world of medical devices is rapidly changing. In place of disconnected, simple medical devices, a new world of complex software both on and off the now-connected device is providing a larger ...

Cambridge, UK - Regulatory compliance in medical device development is often treated as a hurdle to be cleared late in a programme. In practice, addressing it too late can introduce significant ...

At MD&M West 2026, Carl Douglass cuts through the hype to show how additive manufacturing truly accelerates Class II and III ...

Today’s medical devices are very sophisticated, with more providers serving applications in software as well as hardware. These devices are becoming more intelligent and can be tailored to be ...

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 ...