13th Medical Device Safety Monitoring Reporting and Surveillance

13th Medical Device Safety Monitoring Reporting and Surveillance is focused on future medical device regulatory implications for post-market management, risk management, and clinical evaluations, while providing strategies for developing innovative safety and reporting processes.

Topics

• Systematic Literature Review to Support Post-Market Literature Surveillance
• Information That Defined Requirements for Timely EU MDR Submission
• Methods and Resources for Post Market Data Collection and Analysis
• Post Market and Clinical Reporting Deliverables
• Additional Requirements for Clinical Evaluation Imposed by EU MDR
• Novel Approaches to Data Collection, Signals and Trends to Optimize Compliant Management

Who should Attend

Senior level executives from medical device companies with involvement or responsibilities in Quality Assurance, Regulatory Affairs, Medical Device Reporting, Quality Systems, Product Surveillance, Post-Market Surveillance, Clinical Affairs and Product Monitoring.