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:
- Keegan Boyd, Partner, BLG
- Don Boyer, President, BOYER@RegulatorySolns
- Edona Vila, Partner, BLG
