Grand Rounds: Investigator Responsibilities in Clinical Trials
Marie Rape, RN, BSN, CCRC Associate Director, Regulatory ServiceNC TraCS Institute Objectives: Understand the role & responsibility of the PI in Good Clinical Practice Recognize FDA’s requirements and expectations for PI oversight, PI responsibilities Create process to document PI oversight and supervision of research 321 MacNider HallThursday, March 15, 2018, 8:00 AM Sponsored by the … Read more