After IRB Approval…Keeping Your Study Compliant
CCTS Clinical Research Investigator Seminar Series
March 28, 2025
12:00 PM - 1:00 PM America/Chicago
Location
Virtual via Zoom
Calendar
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What investigators need to know and how to prepare when their study is selected for monitoring. Review and discussion of the Clinical & Human Subject Research Compliance program’s purpose and process to assist investigators in maintaining study compliance.
Speaker
Erin Vidra, MS, CHRC
Director, Clinical & Human Subject Research Compliance
Office of Vice Chancellor for Research
About this Series
Co-sponsored by the University of Illinois Cancer Center, the Clinical Research Investigator seminar series is intended to provide faculty investigators with information and skills needed to conduct clinical research at UIC at all stages of a study’s lifecycle.
Date posted
Mar 3, 2025
Date updated
Mar 3, 2025