Advarra eReg
Connecting the clinical research ecosystem.
Overview
Advarra eReg is an electronic regulatory management system designed to help clinical research sites manage documents, compliance, and workflows. As part of Advarra's broader suite of solutions, it integrates with their IRB, IBC, and CTMS offerings to create a more connected research environment.
✨ Key Features
- Electronic Regulatory Binders (eISF)
- 21 CFR Part 11 Compliant Signatures
- Remote Monitoring
- Document Management
- Integration with Advarra CTMS and IRB
🎯 Key Differentiators
- Deep integration with the broader Advarra ecosystem (IRB, IBC, CTMS)
- Strong focus on institutional and site-level compliance
- Backed by Advarra's extensive regulatory expertise
Unique Value: Offers a uniquely integrated solution for sites, connecting eRegulatory management directly with IRB review and CTMS operations to reduce redundant effort and improve compliance.
🎯 Use Cases (4)
✅ Best For
- Used by research sites, academic medical centers, and health systems that also utilize Advarra's other services.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Sponsors looking for an eTMF solution
- Sites that have no other engagement with the Advarra ecosystem
🏆 Alternatives
Provides a more unified and seamless experience for sites already using Advarra's IRB or CTMS, compared to standalone eISF products.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
Free tier: N/A
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