Signant Health TrialConsent
The evidence generation company.
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)
✅ 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
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
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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