Medidata eConsent
The Leading Global Provider of Clinical Development Solutions.
Overview
Medidata eConsent is an electronic informed consent system designed for clinical trials. It is part of the broader Medidata Rave platform, which provides a unified suite of tools for clinical trial management, including EDC, CTMS, and patient-facing solutions. Medidata eConsent aims to improve patient comprehension and engagement through multimedia and interactive content while ensuring regulatory compliance.
✨ Key Features
- Multimedia capabilities (video, images)
- Interactive quizzes to assess understanding
- Remote and on-site consenting
- Unified with Medidata Rave EDC
- Compliant with 21 CFR Part 11, HIPAA, GDPR
🎯 Key Differentiators
- Part of a deeply integrated, end-to-end clinical trial platform (Rave)
- Extensive data and analytics capabilities from a vast number of historical trials
- Strong global presence and support
Unique Value: Provides a unified and data-driven platform that connects all aspects of a clinical trial, from consent to data capture and analysis, reducing friction and providing powerful insights.
🎯 Use Cases (3)
✅ Best For
- Decentralized and hybrid clinical trials
- Global trials requiring multiple languages
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Small, independent research sites
- Investigator-initiated studies with limited budgets
🏆 Alternatives
Offers a more comprehensive and unified suite of tools compared to point solutions, eliminating the need for complex integrations between EDC, eConsent, and other core systems.
💻 Platforms
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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