Informed consent is the communication process through which a researcher explains the details of the clinical trial or research study to a potential research subject, ensures that the information is communicated in a way that is readily understandable to the potential subject, and obtains agreement from that person to participate in the trial/study. It is not just a bureaucratic step, but rather a critical part of human subjects research.
This session will focus on regulatory requirements, special considerations, and the active process of obtaining consent.
Presented by Cheryl Danton, Managing Director, Social & Behavioral Sciences Institutional Review Board (SBS IRB)
Presentation will be followed by Q&A.
Event Details
Wednesday, February 22, 2023, 12:30–1:30pm CST
Zoom Webinar
Open to faculty, postdocs, graduate students, and research staff