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?

It’s simply not enough to mention there is a gap between R&D and manufacturing. There must be some practical steps to be put in place to overcome these issues if a company wants to be successful in ...

The global market for contract manufacturing of medical devices is estimated to grow from $96.4 billion in 2025 to reach $155.2 billion by 2030, at a compound annual growth rate (CAGR) of 10% from ...

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 ...

Many medical implantable devices fabricated using additive manufacturing (AM) technology are already in use in the medical field. The figure shows the clinical application of AM in medical metal ...

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 ...

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 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 ...

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?

MD&M West 2026 exhibitors include medical device contract manufacturers (CMOs), design firms, suppliers, vendors, other ...