Dublin, June 28, 2024 (GLOBE NEWSWIRE) -- The "The US FDA QMSR Transition - 21 CFR 820 and ISO 13485" training has been added to ResearchAndMarkets.com's offering. The US FDA, after years of ...
Dublin, Feb. 24, 2025 (GLOBE NEWSWIRE) -- The "Non-Conformance and Corrective Action for Medical Device Manufacturers Training Course" has been added to ResearchAndMarkets.com's offering. The ...
The company was certified in 2009 to the stringent ISO 13485 standard that requires demonstrating a comprehensive management system for the design and manufacture of medical devices. The FDA 21 CFR ...
DUBLIN--(BUSINESS WIRE)--The "Cybersecurity and US FDA Requirements - Webinar" webinar has been added to ResearchAndMarkets.com's offering. There are regulations such as 21 CFR Part 11 in the U.S. and ...
Manufacturing sites should prepare now for inspections before the U.S. Food and Drug Administration (FDA) resumes routine on-site inspections. Since 2020, FDA has delayed many routine inspections due ...
The "The US FDA QMSR Transition - 21 CFR 820 and ISO 13485" training has been added to ResearchAndMarkets.com's offering. The US FDA, after years of discussing the harmonization of 21 CFR 820, Device ...
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