13th Medical Device Safety Monitoring Reporting and Surveillance

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March 26, 2025 - March 28, 2025

Identify Information That Defined Requirements for Timely EU MDR Submission, Streamline Systematic Literature Review to Support Post-Market Literature Surveillance, Align Post Market and Clinical Reporting Deliverables, Identify Novel Approaches to Data Collection, Signals and Trends to Optimize Compliant Management

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