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Medical Device Roundtable: Post-Market Surveillance Obligations
November 18 @ 10:00 am - 10:30 am
Join us for BLG’s Medical Device Roundtable!
From medical device manufacturers and importers to hospitals and health professionals, in this webinar, the panel of regulatory and legal experts will cover 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.
Want to participate? Please submit the questions you would like addressed through the RSVP form link.