Medrio eConsent
eClinical solutions for every trial.
Overview
Medrio eConsent is designed to simplify the informed consent process for participants, sites, and sponsors. It offers a flexible, intuitive interface for remote and on-site consenting. As part of the Medrio eClinical suite, it integrates seamlessly with their Electronic Data Capture (EDC) and ePRO solutions, providing a unified platform for patient data collection from the very beginning of a study.
✨ Key Features
- Simple drag-and-drop form builder
- Remote and on-site signing
- Direct integration with Medrio EDC
- 21 CFR Part 11 compliant
- Real-time reporting on consent status
🎯 Key Differentiators
- Speed and ease of study setup
- User-friendly interface requires less training
- Unified platform for EDC, eConsent, and ePRO
Unique Value: Delivers a fast, flexible, and easy-to-use platform for data capture and consent, enabling researchers to build and deploy studies in days, not months.
🎯 Use Cases (3)
✅ Best For
- Fast-paced clinical trials that require rapid study build and deployment
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Users who are not using or planning to use the Medrio EDC system
🏆 Alternatives
Prioritizes speed and simplicity over the exhaustive feature sets of larger, more complex enterprise systems, making it a better fit for less complex or time-sensitive trials.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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