🗂️ Navigation

Veeva ePRO

Modern and patient-centric electronic patient-reported outcomes.

Visit Website →

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)

Patient-reported outcomes (PROs) Electronic diaries Symptom tracking Quality of life assessments Hybrid and site-based trials

✅ 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

Web

🔌 Integrations

Veeva Vault EDC Veeva Vault Coder Veeva SiteVault Veeva eConsent

🛟 Support Options

  • ✓ Email Support
  • ✓ Phone Support
  • ✓ Dedicated Support (Enterprise tier)

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ ISO 27001 ✓ SOC 1 Type II ✓ SOC 2 Type II ✓ GxP ✓ 21 CFR Part 11

💰 Pricing

Contact for pricing
Visit Veeva ePRO Website →