Presenter: Julie Mitchell, MPH
December 16, 2021
12 p.m. to 1 p.m.
Part 2 will continue the discussion of Adverse Event data collection and management best practices. The goal of collecting AE data is to monitor patient safety, regulatory compliance, and to answer questions about the safety of the study intervention/procedures. With these goals in minds, this seminar will include collecting data (minimum information needed, methods), coding AEs, grading AEs, and attribution. We will also discuss managing (identifying and correcting) duplicate reports, missing data, and follow-up information/corrections to ensure data integrity. You may view part 1 here.
If you have a disability and need an accommodation to attend or participate in this event, please contact Natalie Lovelace (email@example.com, 503-494-1655) at least five business days before the event.