eREG - A Paperless Regulatory Application to Replace the Traditional Physical Regulatory Binder

The purpose of Advarra's eRegulatory Management System  - eREG is to enhance regulatory compliance, save money, and improve efficiency across UMass Chan research efforts with a 21 CFR Part 11-compliant system designed to adapt to regulatory workflows for all institutional Clinical Research, no matter a study's scale.

eREG – eRegulatory Management System implements a paperless regulatory process for UMass Chan Clinical Trials. The eREG application facilitates the organization, storage, timely access, notification, routing,  signing, and approval of study documents and is the fulcrum to successful study management. eREG works with OnCore, our Clinical Trial Management System, and provides an efficient, cost-effective, enhanced regulatory compliance process across the UMass Chan Research Community.

Research Technology Services
The Research Technology group provides technical support to eREG Users, including:

• Support the Center for Clinical and Translational Science and the Office Of Clinical Research
• Facilitate end-user eREG training account setup
• Provision eREG User Accounts
• Manage the eREG Application and Integrations

For additional information about eREG reach out to the Center for Clinical and Translational Science or visit the Center for Clinical and Translational Science at CCTS LINK.