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13th Medical Device Safety Monitoring Reporting and Surveillance

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March 26 - March 28

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

Details

Start:
March 26
End:
March 28
Website:
https://www.marcusevans.com/conferences/meddevreporting?utm_source=mp&utm_medium=clocate&utm_campaign=chc1150med&utm_id=chc1150
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10x Medical Device Conference
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