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Signant Health TrialConsent

The evidence generation company.

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Overview

Signant Health's TrialConsent is an electronic informed consent solution designed to enhance patient understanding and compliance in clinical trials. It supports various formats, including on-site, remote, and tele-consent, and can incorporate multimedia elements. The platform is built for global deployment, with robust language and localization support, and is part of Signant's broader suite of patient-centric trial solutions.

✨ Key Features

  • On-site, remote, and tele-consent models
  • Multimedia integration
  • Patient comprehension assessments
  • Scalable for global trials with extensive language support
  • 21 CFR Part 11 and GDPR compliant

🎯 Key Differentiators

  • Deep scientific and regulatory expertise
  • Focus on patient-centricity and usability
  • Proven scalability for the largest global trials

Unique Value: Combines scientific expertise with patient-centric technology to ensure high-quality data and a better participant experience in complex global trials.

🎯 Use Cases (3)

Global pharmaceutical trials Decentralized and hybrid trials Studies with complex protocols

✅ Best For

  • Large-scale vaccine trials
  • Oncology and rare disease studies

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Single-site, low-budget academic research

🏆 Alternatives

Medidata Advarra Suvoda

Offers a more specialized focus on patient-generated data (eConsent, eCOA) compared to broad, EDC-centric platforms, often with deeper scientific input into the solution design.

💻 Platforms

Web iOS Android

✅ Offline Mode Available

🔌 Integrations

EDC systems CTMS eCOA/ePRO platforms

🛟 Support Options

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

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ 21 CFR Part 11

💰 Pricing

Contact for pricing
Visit Signant Health TrialConsent Website →