Veeva ePRO
Modern and patient-centric electronic patient-reported outcomes.
Overview
Veeva ePRO is a solution for collecting patient-reported outcomes directly from patients through a web-based application. It is part of the Veeva Vault Clinical Data Management Suite (CDMS), which provides a unified solution for all trial data, including EDC, coding, and data cleaning. This integration allows for a single source of truth for patient and site data. The platform is designed to be patient-centric and easy to use, accessible from any device with a browser, eliminating the need for patients to download a separate application. Study builders can create and deploy ePRO surveys from within the Vault CDMS studio.
✨ Key Features
- Unified with Veeva Vault CDMS
- Web-based, no app required
- Accessible on any device (phone, tablet, computer)
- Build ePRO surveys within the EDC design tool
- Real-time data availability for review
- Automated patient notifications
🎯 Use Cases (5)
✅ Best For
- Phase I-IV clinical trials
- Medical device trials
- Post-market studies
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Studies requiring offline data capture on a native mobile application.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Enterprise tier)
🔒 Compliance & Security
💰 Pricing
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