Seminar Description

Monitoring adverse events (AEs) during the conduct of a study is critical to participant safety.  Clinical research/trials should have data management plans for AE data collection and management throughout the lifecycle of the clinical trial to ensure compliance with good data management practices and institutional and federal reporting requirements.  Presenters will review best practices for standardizing AE descriptions, relatedness, severity, tracking, and reporting. 

If you have a disability and need an accommodation to attend or participate in this event, please contact Natalie Lovelace (lovelacn@ohsu.edu, 503-494-1655) at least five business days before the event.