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:
- Biomedical, Social & Behavioral Basic Human Subjects Course (UICOM-P options) or Human Subject Research (HSR) Course (OSF option)
- Conflict of Interest
- Good Clinical Practice (ICH Focus) (GCP)
- 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).