This webinar brought to you by Zenith PV will provide an overview of Health Canada requirements for MDI reporting, including regulatory expectations, classification of reportable events and practical compliance considerations.
Learning Objectives:
- Understand HC regulatory requirements for MDI reporting under the Medical Devices Regulations (SOR/98-282)
- Identify and classify reportable vs non-reportable incidents using practical examples
- Apply best practices for incident management, documentation, escalations and reporting timelines
Who Should Attend:
- Canadian Medical Device Manufacturers, Importers and License Holders
- Global Medical Device Manufactures and License Holders with distribution operations in Canada
- Medical Device Vigilance and PV Professionals involved in the surveillance and maintenance of medical device safety monitoring activities
Speaker:
Belce Cilmi Arslan, Manager, PV Operations, Zenith PV
