Self-paced, online training
Medical Device Online Training
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Implementing ISO 13485:2016
This course will introduce the requirements of ISO 13485 and outline the steps for building an ISO 13485 compliant quality management system.
Introduction to ISO 13485 & FDA QSR
This course is for professionals in the medical device industry who want to learn about ISO 13485. Gain experience and a deeper understanding of the ISO 13485 Standard and requirements.
European Medical Devices Regulation (EU MDR) Training
The European Medical Devices Regulation (EU MDR) applies to all manufacturers of medical devices sold in Europe. Gain an understanding of the EU MDR and how the new requirements will affect your organization.