Description:

This presentation will cover special topics when obtaining informed consent, including identifying circumstances that may arise during the consent process for certain populations, how to address these circumstances, and regulatory issues specific to these populations.

Speaker: 

Darlene Kitterman, Director, Clinical Trials Office, UI Cancer Center

Arielle Breanna Guzman, Senior Clinical Research Coordinator, Clinical Trials Office, UI Cancer Center

RC+ Program: Core Competency  #2: Ethical and Participant Safety Considerations

Contact: Sudeshna De, ccts-training@uic.edu