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Medical Device Roundtable: Post-Market Surveillance Obligations

From medical device manufacturers and importers to hospitals and health professionals, in this webinar, the panel of regulatory and legal experts covered the following:

  • 2021 updates to the Medical Devices Regulations on post-market surveillance obligations of medical device license holders;
  • Reporting obligations to Health Canada on adverse incidents involving medical devices sold and imported into Canada; and
  • Use of post-market surveillance regulatory disclosure in medical device litigation and cross-border issues.

Our Speakers:

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Key Contacts