BOSTON--(BUSINESS WIRE)--908 Devices, a pioneer of purpose-built analytical devices for chemical analysis, today announced that it has achieved the ISO 9001:2015 certification. This latest edition of ...
Medical device companies MUST have established risk management processes that comply with ISO 14971. And it doesn’t matter if you are developing medical devices in the U.S., EU, Canada, and so on. ISO ...
Dublin, Jan. 27, 2026 (GLOBE NEWSWIRE) -- The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (May 21, 2026)" training has been added to ...
Dublin, Jan. 29, 2026 (GLOBE NEWSWIRE) -- The "Sterilization of Medical Devices Training Course (Apr 23rd - Apr 24th, 2026)" training has been added to ResearchAndMarkets.com's offering. Sterile ...
—Leading manufacturers of consumer-oriented medical devices certify ModusLink according to their ISO-based quality systems— WALTHAM, Mass.--(BUSINESS WIRE)-- ModusLink Global Solutions ™ Inc. (NASDAQ: ...
Significant quality systems and product requirements must be satisfied by manufacturers to ensure their medical devices produced are fit for their intended purpose, ISO notes, recognizing the wide ...
The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers ...
ISO 14971 provides a framework for medical device manufacturers to identify and minimize risks through the design and manufacturing processes. Adhering to the standard helps ensure overall safety and ...
DONGGUAN, GUANGDONG, CHINA, January 13, 2026 /EINPresswire.com/ -- As healthcare moves toward proactive and at-home ...
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