The publication of ISO 13485:2016 marked a significant advancement in Quality Management Systems (QMS) for organisations involved in the lifecycle of medical devices. Specifically designed to support medical device manufacturers, this standard provides a robust framework for establishing and maintaining effective processes to ensure the consistent design, development, production, installation, and delivery of medical devices that are safe and fit for their intended use. A formal review in 2020 confirmed that the 2016 version remains current and valid.
This expertly developed, interactive online course—updated in 2020—offers a comprehensive exploration of ISO 13485:2016 and its practical application in real-world settings. Learners will build their knowledge through engaging, scenario-based activities and interactive content designed to reinforce key concepts.
Upon successful completion, participants will be equipped to contribute to the development, implementation, and maintenance of an ISO 13485:2016-compliant Quality Management System and support continued regulatory compliance and certification within their organisation.
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Click the link above to explore the complete course content in our PDF leaflet.
