Webinar Description:
The Medical Devices Compliance Verification Program (MDCV) of the Regulatory Operations and Enforcement Branch oversees post-market compliance and enforcement of medical devices. The program investigates potential health hazards and regulatory violations via mandatory problem reports, voluntary industry reports, complaints, recalls, and ad-hoc requests.
The presentation provides an overview of the MDCV program including:
- Triaging and prioritizing complaints and recalls
- Monitoring recalls and conducting compliance verification
- Key tools and activities used in compliance verification
- What to expect when a CV inspector contacts you
Speakers:
Niraj Patel
Jasmin Poirier
Regional Regulatory Compliance and Enforcement Specialists
Medical Devices Compliance Verification Program
Regulatory Operations and Enforcement Branch
Have Questions?
Be part of the conversation. Submit your questions in advance to info@diac.ca by October 15, 2025. Please use the subject line "Question for Compliance Verification".
Registration Fee:
Free for DIAC members | $99 for non-members (fee credited if you join DIAC).
Registration Deadline:
Closes at 1:00 PM on October 21, 2025.
