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Canada Medical Device Regulations – a Comprehensive Overview

NSF International
Training overview
2 hours
399 USD
Next start date: Inquire for more information - Online

Course description

Canada Medical Device Regulations – a Comprehensive Overview

This course comprehensively covers regulatory requirements including the regulatory framework, pre and post market requirements, and instruction on the way Canada is utilizing MDSAP.

Training Content


By the end of this course, you should:

  • 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 premarket pathway and requirements for medical devices.
  • Understand the Quality Management System regulations required to market a medical device.
  • Understand the post-market requirements for medical devices.

For more information Visit University Website.

Certification / Credits


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

About supplier

NSF International

NSF International

NSF Health Sciences partners with life science companies, big and small, to provide highly customized end-to-end services throughout the product lifecycle. From early development to commercial manufacture and distribution, our expert services will assist you to: Ensure regulatory compliance Implement...

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