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Adverse Event Reporting: Trials and Tribulations

Adverse Event Reporting: Trials and Tribulations. Joanne R. Less, Ph.D. Director, IDE and HDE Programs ODE, CDRH, FDA Second Annual Medical Research Summit Grand Hyatt Hotel March 26, 2002. Adverse Event Reporting: Trials and Tribulations. I. Definitions and Reporting Requirements

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Fda promptly section 56 - PowerPoint PPT Presentation

Adverse Event Reporting: Trials and Tribulations