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.
Our Speakers:
- Keegan Boyd, Partner, BLG
- Don Boyer, President, BOYER@RegulatorySolns
- Edona Vila, Partner, BLG
Want to participate? Submit the questions you would like addressed through [email protected]. Please RSVP by November 17.
CPD Details
BC | This course has been accredited for 0.5 hour. Course name: Medical Device Roundtable: Post-Market Surveillance Obligations. Course number: N18112021.
ON | This session is eligible for up to 0.5 Substantive Hour.
QC | Please note, the concept of "recognition" or "accreditation" has been abolished. By doing this, the Barreau is trying to make it easier for lawyers to claim mandatory CLE credits without a formal accreditation process. It is now up to individual lawyers to determine the eligibility of a training activity and to declare the hours in their “Dossier de formation en ligne”.
