Advarra eReg allows all types of research sites to improve efficiency, accelerate study startup, and enhance regulatory compliance across their organization. Developed in close collaboration with academic medical centers, cancer centers, health systems, sites, and site networks, eReg allows you to: Quickly and efficiently route documents, automatically alert staff when new documents are available, facilitate electronic signatures, and more Easily and securely allow remote access to sponsors and monitors Improve study startup timelines by automating document exchange with sponsors and CROs Integrate with your existing technology, including OnCore and Clinical Conductor CTMS, eIRB, Advarra’s Longboat and CIRBI platforms, and email systems