The goal of this course is to provide CRS staff with training on how to assess Adverse Events (AEs) using the Manual for Expedited Reporting of Adverse Events to DAIDS (EAE Manual), and how to use the DAIDS Adverse Experience Reporting System (DAERS) to report EAEs to DAIDS. This abbreviated course is for CRS staff participating in therapeutic trials and need expedited access to DAERS. All other CRS staff should complete the full longer course.