SITE TECHNOLOGY
eReg
Think Beyond the Binder
Save money, improve efficiency, and connect to technology across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory workflows for any size research site.
Connected, Paperless eRegulatory Management
Improve your routing and workflows
Quickly and easily route documents, automatically alert staff when new documents are available, and boost regulatory compliance and efficiency with electronic signatures for protocol documents, delegation of authority, and more.
Integrate with your enterprise systems
Improve productivity and compliance by integrating eReg with Advarra’s CIRBI platform, eIRB systems, OnCore, Clinical Conductor, your internal email system, and even a sponsor electronic trial master file (eTMF).
Easily and securely allow remote access to sponsors and monitors
Allow monitors to conduct fully remote monitoring visits and source document verification during a specified time using Advarra eReg’s remote monitoring capabilities.
Apply shared documents and records across multiple protocols
Create standard templates for protocol-essential documents tailored to each study type (National Institutes of Health [NIH], industry, European Medicines Agency [EMA], etc.) to use repeatedly, and share staff credentials across multiple protocols.
Move beyond paper binders
Save staff time, effort, and money when easily storing signed consent forms, contact information, compensation records, investigational new drugs (INDs), and more. Centralize your organization’s standard operating procedure (SOP) document storage and management, allowing quick access for internal staff and sponsor monitors.
Efficiently and compliantly manage multi-site trials
As a coordinating center, view and manage protocol documents for participating sites in an investigator-initiated trial. Plus, leverage eReg’s master delegation of authority capabilities to significantly reduce the amount of time spent routing and obtaining signatures on documents.
The Trusted eReg Platform for Research Sites
Connecting Sites and Sponsors
Secure Document Exchange allows all regulatory documents, originating with a sponsor or at a site, to be managed, signed, and securely exchanged seamlessly within the investigator site file (ISF) (eReg) or sponsor electronic trial master file (eTMF). Read about our approach and how industry-wide collaboration is the key to solving this longstanding challenge.
Case Studies
Duke University Prioritizes Advarra eReg’s Site Centric Workflows Within a Connected Research Ecosystem
The James Comprehensive Cancer Center at The Ohio State University Boosts Compliance and Productivity with Advarra eReg
Inova Health System Uses Advarra eReg Workflows and Integrations to Improve Regulatory Efficiency
