Human Subjects Training
All investigators, staff and students with Human Subjects training greater than three years old (from any training source) are required to update their training through the CITI Training module. All new protocol submissions may be held for approval until the training has been updated. Please note that all personnel listed on protocols must complete the human subjects training.
Responsible Conduct of Research
Responsible Conduct of Research training is required for certain NIH, NSF, and NIFA funded projects but is not the same as the Human Subjects Training course. The correct course in CITI is called "IRB Investigators and Student Researchers". Please refer to the registration instructions to the right for help on selecting the correct course or contact the IRB Coordinator. Visit the Responsible Conduct of Research page for more information on this training requirement.
Clinical Trials and Good Clinical Practice (GCP)
Effective January 1, 2017, all NIH-funded clinical investigators and clinical trial staff who are involved in the design, conduct, oversight, or management of clinical trails are required to complete the Good Clinical Practice (GCP) training. There are 4 courses available in the CITI program tailored to the different types of clinical research. Please refer to the site for more information on this training requirement.
Please contact the IRB Coordinator at 111-111-6340 with any questions.