PI Responsibilities and the 1572

This course provides an overview of the PI's responsibilities for managing adverse events in a clinical trial. Dr. Paul Martin reviews key definitions, distinguishes between the terms "severe" and "serious," and examines how adverse events should be assessed and documented.

Author: Fred Hutch Clinical Research Support (CRS) with Paul Martin, MD

RC LEVEL 1, 2, 3

This opportunity is open to all eligible persons regardless of race, sex or other identity.