CITI Training Requirements for Authorized Study Personnel

Effective April 1, 2018: The UICOM-PIRB IS changing the CITI training requirements related to Human Subject Research. The UICOM-P IRB has adopted the following CITI training requirements effective 4/1/18 for any new study, continuing review, or addition of authorized study personnel:

  1. Biomedical, Social & Behavioral Basic Human Subjects Course (UICOM-P options) or Human Subject Research (HSR) Course (OSF option)
  2. Conflict of Interest
  3. Good Clinical Practice (ICH Focus) (GCP)
  4. Responsible Conduct of Research (RCR)

Investigators can access CITI training at citiprogram.org.

Effective January 1, 2017: NIH Policy requires Good Clinical Practice (GCP) training for all NIH-funded investigators and staff who are involved in the conduct, oversight, or management of clinical trials. The UICOM-PIRB CITI GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus) fulfills this requirement.

Effective March 2016: The UICOM-PIRB made available additional CITI training courses related to Good Clinical Practice (GCP) and Responsible Conduct of Research (RCR).

Contact Us

Peoria Institutional Review Board

One Illini Dr.
Peoria, IL 61605

Phone: 309-680-8630
Fax: 309-671-3406