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Advarra Longboat eConsent

Connecting the clinical research ecosystem.

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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)

Pharmaceutical and biotech sponsors Contract Research Organizations (CROs) Large research institutions

✅ 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

Signant Health Medidata Florence

Unlike pure technology vendors, Advarra provides an integrated solution of technology and expert services, streamlining the entire study start-up and compliance process.

💻 Platforms

Web iOS Android

✅ Offline Mode Available

🔌 Integrations

Advarra IRB Platform CTMS EDC

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ SSO ✓ 21 CFR Part 11

💰 Pricing

Contact for pricing
Visit Advarra Longboat eConsent Website →