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 ...
The U.S. FDA’s emphasis on internationalized regulations continues with the agency’s adoption of ISO 14971, the risk management framework published by the International Organization for ...
Dublin, Sept. 29, 2025 (GLOBE NEWSWIRE) -- The "An introduction to Risk Management ISO 14971:2019 Training Course (Nov 11, 2025)" training has been added to ResearchAndMarkets.com's offering.
In the wake of rising cases of medical device software defects and malfunctions, software quality assurance and compliance with regulation has come to the forefront of discussion among industry ...
This 90-minute webinar on Advanced Methods of Root Causes Analysis, for medical device companies, will cover principles and methods of Root Cause Analysis (RCA) and review proven techniques for ISO ...
This course provides the attendees with an overview of ISO 14971:2007 and implementation tips for an effective system for managing risk. We provide an overview using flow charts that shows each of the ...
The U.S. FDA’s emphasis on internationalized regulations continues with the agency’s adoption of ISO 14971, the risk management framework published by the International Organization for ...
Dublin, April 12, 2023 (GLOBE NEWSWIRE) -- The "Risk Management in the Medical Device Industry - Understand Iso 14971" training has been added to ResearchAndMarkets.com's offering. Medical Devices by ...
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