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Good Clinical Practice

All investigators and key research personnel engaged in human subject Clinical Trials research (proposals involving drugs, devices, interventional/behavioral treatments) must complete the online Collaborative Institutional Training Initiative (CITI) program for Good Clinical Practice (GCP) prior to IRB approval of a new or continuing review application.

Key research personnel are defined as the Principal Investigator, other investigators and research personnel who are directly involved in conducting research with study participants or who are directly involved with the clinical trial, or handling private information (patient's medical records and charts) related to study participants during the course of a research project. Key research personnel also include faculty sponsors who provide direct oversight of research with study participants or research using study participant's private information.