Join us for BLG’s Medical Device Roundtable!
From medical device manufacturers and importers to hospitals and health professionals, in this webnar, 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.

Our Speakers:

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

Want to participate? Please submit the questions you would like addressed through the RSVP form link below.

RSVP