CRIO (Clinical Research IO)
The future of clinical trials is here.
Overview
CRIO is a modern, integrated platform designed for clinical research sites. It started with a focus on tablet-based eSource for paperless data capture and has expanded to include full CTMS and eRegulatory functionalities. CRIO is praised for its user-friendly interface and its ability to create efficient, paperless workflows for sites.
✨ Key Features
- Electronic Source (eSource) for direct data capture
- Integrated Clinical Trial Management System (CTMS)
- Electronic Regulatory (eRegulatory) binders
- Patient recruiting and scheduling
- Financial management and stipend tracking
- Real-time data access for remote monitoring
- 21 CFR Part 11 compliant electronic signatures
🎯 Key Differentiators
- Pioneering eSource solution designed by clinical researchers for sites
- Intuitive, user-friendly interface to drive site adoption
- Integrated platform covering eSource, CTMS, and eRegulatory
Unique Value: Empowers clinical research sites to be more efficient and compliant by replacing paper-based processes with a single, intuitive electronic system for data capture and site management.
🎯 Use Cases (3)
✅ Best For
- Independent research sites and site networks focused on operational efficiency.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Sponsors looking for a global portfolio management and oversight tool.
🏆 Alternatives
Offers a more integrated and user-friendly eSource solution compared to traditional EDC systems that require double data entry, or CTMS systems that lack robust source data capabilities.
💻 Platforms
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Live Chat
- ✓ Phone Support
- ✓ Dedicated Support (All tier)
🔒 Compliance & Security
💰 Pricing
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