OCTRI Research Forum: Adverse Event Data Management Best Practices
Presented by: Cynthia Morris, PhD & Julie Mitchell, MPH
When |
October 21, 2021 to October 28, 2021
12 p.m. to 1 p.m.
Seminar DescriptionMonitoring 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. |
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Where |
VIRTUAL |
Contact Information |
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.