CRISS Series: “After IRB Approval…Keeping Your Study Compliant”
Date / Time
March 28, 2025
12:00 pm - 1:00 pm
Categories
What investigators need to know and how to prepare when their study is selected for monitoring. Review and discussion of the Clinical and Human Subject Research Compliance program’s purpose and process to assist investigators in maintaining study compliance.
Speaker:
Erin Vidra, MS, CHRC
Director, Clinical and Human Subject Research Compliance
Office of Vice Chancellor for Research
The Clinical Research Investigators Seminar Series is intended to provide faculty and other investigators with information and skills needed to conduct clinical research at UIC at all stages of a study’s lifecycle.
Register for the online training.
For more information, email ccts-training@uic.edu.
