Attendees will learn best practices for organizing, maintaining, and retaining research records to ensure regulatory compliance, data integrity, and audit readiness throughout the lifecycle of a research study. You will gain practical knowledge on managing regulatory binders, documenting research activities, maintaining participant records, and applying Good Clinical Practice (GCP) principles to both paper and electronic research documentation systems.
If you are obtaining PSNA credits, you can miss no more than 10 minutes of the presentation and your camera must remain on.
