XIANYANG CITY, SHAANXI PROVINCE, CHINA, January 21, 2026 /EINPresswire.com/ -- The pharmaceutical ingredients and ...

Simpler rules apply to less invasive hardware ...

FDA's new medical device quality management rules align U.S. standards with global requirements and give inspectors new ...

Resolution Medical’s devices are for medical technology end markets including structural heart, cardiology and vascular, electrophysiology, and neuromodulation therapies Resolution Medical was founded ...

Additive manufacturing (AM) has become a powerful tool for accelerating regulated medical device development. Yet its value hinges on how and when it’s applied. At the MD&M show in Anaheim, CA, Carl ...

Single-use medical devices (SUDs) and sustainable practices are not mutually exclusive, but finding common ground is not a simple proposition. There is no question that SUDs have contributed to ...

The FDA has eliminated a key barrier to the use of real-world evidence in certain medical device applications. Under new guidance issued Dec. 15, the agency said it will accept real-world evidence ...

The FDA now accepts RWE for device submissions without needing identifiable patient data, facilitating the use of large, de-identified databases. This change addresses previous limitations that ...

ProPublica is a nonprofit newsroom that investigates abuses of power. Sign up to receive our biggest stories as soon as they’re published. The Food and Drug Administration rarely uses its authority to ...

At a time when medical technology breakthroughs often stall long before reaching patients, Northwestern University’s Querrey Simpson Institute for Bioelectronics (QSIB) has become a striking exception ...

Expertise from Forbes Councils members, operated under license. Opinions expressed are those of the author. So, it’s probably a great time to revisit what I thought was going to shape the industry in ...