45 mins

EU Medical Device Regulation (EU MDR) – Chapter 7 – Post Market Surveillance, Vigilance and Market Surveillance

MDSAP Country Specific Requirements (Japan)

ISO 14971:2019: Different Perspectives of a Risk Management Program

MDSAP Country Specific Requirements (Brazil)

ISO 14971:2019: Risk Analysis, Evaluation & Control

MDSAP Country Specific Requirements (Australia)

Commissioning Qualification and Validation the Concept of CQV – Part 3

ISO 14971: Characterizing the Device & Identifying Hazards

EU Medical Device Regulation (EU MDR) – Chapter 6 – Clinical Evaluation and Clinical Investigations

The Lifecycle of a Change Control Program – Phase 3: Implement and Phase 4: Review