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, Oct. 17, 2025 (GLOBE NEWSWIRE) -- The "An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (Nov 20, 2025)" training has been added to ...
TORONTO, ON / ACCESSWIRE / June 22, 2022 / AI/ML Innovations Inc. (CSE:AIML)(OTCQB:AIMLF)(FWB:42FB), a company committed to acquiring and advancing Artificial Intelligence/Machine Learning ...
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 ...
South African Health Products Regulatory Agency (Sahpra) has indicated that ISO 13485 certification is a prerequisite for the application or renewal of a medical-device license, with effect from 1 ...
BROOKFIELD, Wisc.--(BUSINESS WIRE)--Headline of release dated November 6, 2013 should read: InControl Medical: Maker of InTone, Apex and Intensity, Receives ISO 13485 and CE Mark Medical Device ...
CHADDS FORD, Pa., July 29, 2025 /PRNewswire/ -- ClariMed, Inc., a global leader in human-centered medical device development and regulatory services, today announced it has achieved ISO 13485:2016 ...
Barger, a leading medical and pharmaceutical packaging designer and manufacturer, has proven its ability to meet strict international, as well as customer, quality management system (QMS) requirements ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback