eReg Benefits For Clinical Research: Use Cases For All Types Of Sites

By Marmee Lutz, Product Manager

To maintain regulatory compliance throughout clinical research, sites and institutions must ensure that documents are correctly updated and maintained consistently. Completing these tasks can take a significant amount of time away and effort from research teams. To improve workflows, increase productivity, save money, and improve compliance, teams are utilizing eRegulatory systems.

With the right eRegulatory system, any size organization can benefit. Unearth the different kinds of eRegulatory use cases for diverse clinical site types and other eRegulatory capabilities designed to serve all sites. Additionally, look at Advarra’s eRegulatory Management System (eReg), an 21 CFR Part 11 compliant system, designed to adapt to and streamline research site regulatory workflows.