Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

With Covid accelerating time-to-market for medical devices, digital tools play a key role in managing converging priorities ...

We’ve all heard process validation horror stories. Validations can take years. Creeping elegance can take over. Product launches can be stopped in their tracks. When implemented correctly, however, ...

Validfor is excited to announce the launch of its Agentic Digital Validation Platform for life sciences, designed to ...

Facility & Process Validation is a component of the quality assurance framework of pharmaceutical, biotechnology, and medical device manufacturing. It is a process used to evaluate the manufacturing ...

Resonetics experts explain the different stages of nitinol’s journey as it becomes part of a life-changing medical device.

FDA’s 21 CFR Part 820 — Quality System Regulation (QSR) has not been updated since it was first released in 1996 . . . until now. Are you ready? Part of a panel at the conference discussing the ...

Medical device manufacturing is a high-stakes game where efficiency meets precision. With tight regulations, complex designs, and a need for speed, how do companies stay ahead without cutting corners?

The "Sterilization of Medical Devices Training Course (Apr 23rd - Apr 24th, 2026)" training has been added to ResearchAndMarkets.com's offering. Sterile devices are free of viable microorganisms and ...