ChatGPT, an artificial intelligence (AI) tool, has the potential to revolutionize the creation of informed consent forms and related documents for clinical trials. This session focuses on developing concise, participant-centered, and compliant consent forms, and on addressing limitations in sponsor or institutional customization, compliance, and data privacy regulations.
CEU: 1.00 ACRP
Speakers:
Jeri Burr, MS, RN, PED-BC, CCRC, FACRP, Program Director, University of Utah
Ann Johnson, PhD, MPH, IRB & HRPP Director, University of Utah, Institutional Review Board
John VanBuren, PhD, Associate Professor, University of Utah
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