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.

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 ...

At some point, imperfections are likely to creep into every kind of manufactured product. But in the world of medical devices, there’s no margin of error. Does it ...

With stringent regulations and limited cleanroom space, scaling medical device production is no easy feat. Learn how a modular assembly system powered by Rockwell Automation’s MagneMover Lite ...

The evolution of medical-grade thermoplastic polyurethanes (TPUs) continues to reshape possibilities for device manufacturers seeking materials that combine flexibility, durability and ...

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...

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 ...

In this interview, Shira Weiner describes the features and benefits of medical-grade adhesives for medical device manufacturing. What are some of the characteristics of medical-grade adhesives?

A breakthrough development in nanofabrication could help support the development of new wireless, flexible, high-performance ...