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, ...

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

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

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 ...

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 ...

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?

Regulating manufacturing processes in the medical device industry is challenging. But process signature verification can help manufacturers get a handle on problems before they get out of control.

Synthetic urine is engineered to replicate the essential physical and chemical properties of real urine rather than its ...

Device makers are taking increased interest in product designs and assembly that support closed-loop recycling. A Branson plastic welding process can safely and nondestructively “unweld” plastics used ...

Growing adoption of cardiovascular and urological implants, AI-enabled manufacturing, and demand for cost-efficient care accelerate global market expansion.Austin, Texas, Jan. 28, 2026 (GLOBE NEWSWIRE ...