Advarra's eRegulatory Management System (eREG) is a 21 CFR Part 11 compliant system designed to adapt to and streamline research site regulatory workflows. Features available for use in eREG include routing an signing documents, delegation of authority, applying shared documents across multiple protcols, securely allowing access to sponsors and monitors, managing multi-site trials, and effectively acting as the research binder for study protocols. eREG is able to link with OnCore for protocol management.
eREG is used campuswide for oncology research, and implementation is underway for non-oncology studies. Non-oncology study teams interested in learning more about using eReg for regulatory management, email CTMS-Support@ouhsc.edu, and we will work with you to assess your team's needs and facilitate system access.