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 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?

This edition explores how materials science, nanofabrication, and workforce development intersect to support a resilient U.S.

In a world full of "smart" devices (i.e., smartphones, smart watches, and smart appliances), such technology is increasingly entering manufacturing and processing in forms like condition monitoring, ...

Medical device manufacturing has always been a balancing act between innovation and regulation. For companies specializing in plastic components—whether injection-molded housings, fluid connectors, ...

Although the medical device industry has seen nothing but growth over the past few decades, that same growth has been routinely hindered by the systems and capacities that produce these devices. As ...

Researchers develop a more environmentally friendly approach to manufacturing nano-scale microchip devices using water as a solvent in place of toxic chemicals. The method not only cleans up the ...

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 ...

Supporting global OEM/ODM brands with reliable electronic device housing solutions from design to production. FOSHAN, ...