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 ...

A new master research agreement with C3 Medical Device Consulting supports product development, technology innovation, and ...

Regulated healthcare companies are under increasing pressure to move faster while maintaining the highest standards of ...

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, ...

Some medical technologies are just plain cool. But tech that’s only cool is never enough. It must solve specific health problems, improve each patient’s quality of care, and be easy to use. To create ...

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.

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 ...

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

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 ...

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 ...