Advarra eRegulatory Management System
Streamline Regulatory Processes and Enhance Compliance.
Overview
Advarra's eRegulatory Management System (eReg) is designed to help clinical research sites manage regulatory documents electronically. As part of Advarra's broader ecosystem of IRB, IBC, and consulting services, the eReg system offers deep integration with compliance workflows, helping to ensure inspection readiness and streamline operations.
✨ Key Features
- Electronic Regulatory Binders (eISF)
- 21 CFR Part 11 Compliant
- Integration with Advarra IRB Platform
- Remote Monitoring Support
- Document Management and eSignatures
- Task Management and Workflows
🎯 Key Differentiators
- Integration with the broader Advarra ecosystem of compliance services (IRB, IBC)
- Single vendor for both IRB review and eRegulatory software
- Strong focus on institutional and site-level compliance
Unique Value: Offers a unified platform for managing regulatory documents and IRB submissions, creating a seamless compliance workflow for research sites.
🎯 Use Cases (4)
✅ Best For
- Used by research sites, particularly those already utilizing Advarra's IRB services, to create a more connected compliance environment.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Organizations not involved in clinical research
- Basic academic research grant management
🏆 Alternatives
Provides unique value through its direct integration with Advarra's market-leading IRB services, which competitors cannot offer.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Standard tier)
🔒 Compliance & Security
💰 Pricing
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