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

A significant market opportunity lies in providing comprehensive training on technical documentation for medical device manufacturing, focusing on DHF, DMR, and DHR. This ensures regulatory compliance ...

At MD&M West 2026, Carl Douglass cuts through the hype to show how additive manufacturing truly accelerates Class II and III ...

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

Technologies like chat GPT have become readily available and easy to use on the commercial consumer side of things, said Zakary Tyler Smith, cofounder and CEO of SensFlo, in an interview with MD+DI.

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 ...

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

The "Contract Manufacturing of Medical Devices: Global Markets" report has been added to ResearchAndMarkets.com's offering. The global market for contract manufacturing of medical devices is estimated ...

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 ...

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 ...