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Canada Medical Device Regulations – A Comprehensive Overview

About This eLearning

This two-hour course provides a comprehensive overview of medical device regulatory requirements including the regulatory framework, pre- and post-market requirements, and the way Canada is utilizing MDSAP.


By the end of this course, you will be able to:

  • Identify the regulatory framework for medical devices
  • Determine the correct classification for medical devices
  • Understand how Canada utilizes the Medical Device Single Audit Program (MDSAP)
  • Understand the pre-market pathway and requirements for medical devices
  • Understand the quality management system regulations required to market a medical device in Canada
  • Understand the post-market requirements for medical devices in Canada

Who Should Attend

This course is essential for anyone wanting to bring a medical device or IVD to market in Canada, and also for employees in R&D, regulatory, quality and compliance functions.

Let NSF help you with this Canada medical device regulations course.


By completing/passing this course, you will attain the Medical Device Certificate.