Dublin, April 15, 2026 (GLOBE NEWSWIRE)-- The "Process Validation for Medical Devices (June 4th - June 5th, 2026)" training has been added to ResearchAndMarkets.com's offering. Process validation is ...

Dublin, April 14, 2026 (GLOBE NEWSWIRE)-- The "FDA Approval Process for Medical Devices (June 30, 2026 and July 1, 2026)" training has been added to ResearchAndMarkets.com's offering. Gain a ...

WEST LAFAYETTE, Ind. – A patent-pending process developed by Purdue University engineers could improve the quality of life for the more than 6 million people who undergo orthopedic and trauma surgery ...

BOSTON--(BUSINESS WIRE)--908 Devices Inc., (Nasdaq: MASS), a pioneer of purpose-built handheld and desktop devices for chemical and biochemical analysis, announced that National Resilience, Inc.

BOSTON--(BUSINESS WIRE)--908 Devices (Nasdaq: MASS), a pioneer of purpose-built handheld and desktop devices for chemical and biomolecular analysis, is collaborating with UK-based, deep-tech ...

New process device profiles have been added by ODVA to the EtherNet/IP specification to provide end users with another tool to help optimize plant operations. According to ODVA, the new process device ...

Risk Management is a vital component to developing and designing medical devices. Before your product goes to market, you have to know that it is safe and that you've analyzed and mitigated every risk ...

As noted in Chapter 1, the committee was charged by the Food and Drug Administration (FDA) to review the 510(k) clearance process and answer two principal questions: Does the current 510(k) clearance ...

April 9, 2010 — In its latest effort to reduce the risks of medical radiation, the US Food and Drug Administration (FDA) yesterday notified manufacturers of radiotherapy equipment such as linear ...

A manufacturing process that accelerates the production of fiber-optic components has been patented by Lumenon Innovative Lightwave Technology Inc. of Quebec, Canada. While the fiber-optic industry is ...