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

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 ...

In this free webinar, learn how medical devices benefit from modern digital validation strategies. Attendees will learn how digital validation builds confidence and removes redundancy. The featured ...

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, ...

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 ...

Product design risks can be mitigated through digital commissioning strategies for device design that speed continuous design ...

The main market opportunities lie in addressing the stringent regulatory requirements for sterile medical devices through education on sterilization methods, compliance, and standards. Offering ...

Process validation is crucial for ensuring the quality of final products and the safety of these processes for manufacturing personnel and consumers in the pharmaceutical, medical device, and ...

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