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An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Training Course (ONLINE EVENT: March 13, 2025) - ResearchAndMarkets.com February 20, 2025 07:10 AM Eastern ...
Use this step-by-step guide to comply with ISO 13485 and FDA quality management system (QMS) requirements for medical device companies.
Cognidox, a leading provider of electronic Quality Management Systems (eQMS) for medical device and life science companies, today announced the ...
In addition, compliance with international standards, such as ISO 13485 (medical device quality management) and ISO 14971 (medical device risk management), require ongoing updates to security ...
This certifies the compliance of FineHeart's quality management system with medical device industry regulations and has been issued following an audit by BSI, the independent, internationally ...
As the CEO of a quality management system software company that’s specifically designed for the medical device industry, it should be easy to see why I’m committed to improving the quality of ...
ISO 13485 Medical devices — Quality management systems — Requirements for regulatory purposes is an International Organization for Standardization (ISO) standard.
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