Advarra Longboat eConsent
Connecting the clinical research ecosystem.
Overview
Advarra's Longboat eConsent platform is designed to improve the patient experience and comprehension during the informed consent process. It leverages multimedia and interactive elements to explain complex study information. Being part of Advarra, it benefits from deep integration with compliance and regulatory workflows, including IRB review.
✨ Key Features
- Multimedia and interactive content
- Patient comprehension tracking
- Remote and on-site consent options
- Integration with Advarra's IRB and compliance services
- 21 CFR Part 11 and HIPAA compliance
🎯 Key Differentiators
- Deep expertise in research compliance and IRB workflows
- Focus on patient engagement and comprehension
- Unified platform with other Advarra services
Unique Value: Offers an eConsent solution backed by the industry's leading institutional review board (IRB) and compliance experts, ensuring a highly compliant and patient-centric process.
🎯 Use Cases (3)
✅ Best For
- Complex therapeutic area trials (e.g., oncology)
- Global, multi-language studies
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Small, single-site investigator-initiated studies
🏆 Alternatives
Unlike pure technology vendors, Advarra provides an integrated solution of technology and expert services, streamlining the entire study start-up and compliance process.
💻 Platforms
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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