Keyword: reporting adverse events

Management and Reporting of Adverse Events (AE), Serious Adverse Events (SAE), Unanticipated Adverse Device Effects (UADE), and Unanticipated Problems (UaP) Standard Practice Guideline

Study-specific, local, and federal guidelines for AEs, SAEs, UADEs, and Unanticipated Problems to maintain regulatory congruence and integrity in research practice

Keyword: reporting adverse events

Management and Reporting of Adverse Events (AE), Serious Adverse Events (SAE), Unanticipated Adverse Device Effects (UADE), and Unanticipated Problems (UaP) Standard Practice Guideline

Subscribe to our newsletter