Advarra eRegulatory Management System (eReg) is an electronic regulatory binder maintenance system that allows organizations to store essential protocol documents, staff credentials, and organizational regulatory documents.
To support compliant and efficient consent workflows, the University of Iowa offers a Part 11–compliant electronic consent (eConsent) function within the ICTMS eReg system. This feature is available for FDA‑regulated clinical trials involving drugs and/or devices and is designed to ensure adherence to federal regulations and institutional policies while maintaining a clear, participant‑centered consent process.
Access & Training
Upon completion of the access request form, you will be assigned eReg specific coursework on Advarra University, which is required to be completed prior to granting your user access to eReg.
The ICTMS administrative team will set up your coursework sessions in Advarra University and you will email the step-by-step instructions about how to complete the required coursework.