What is Advarra eReg?
Digitize and streamline your regulatory processes with eReg, a 21 CFR Part 11-compliant system designed to enhance regulatory compliance and workflow efficiency for research sites of any size. Developed in close collaboration with academic medical centers, cancer centers, health systems, sites, and site networks, eReg enables you to optimize document management, accelerate study startup, and facilitate remote access across your organization
Highlights
- Automated document routing, alerting, and electronic signing to improve efficiency
- Secure remote access for sponsors and monitors
- Integration with existing technology, including CTMS, eIRB, and email systems
- Accelerated study startup through automated document exchange with sponsors and CROs