Veeva ePRO | Experience Seamless Data Flow

Veeva ePRO

High-Quality Patient Data When You Need It

Simplify the design, management, and completion of patient reported outcomes

Announced 2022
Status EARLY
Customers 1-10

Veeva ePRO captures questionnaire responses directly from patients to ensure consistent and real-time tracking of success criteria.

Sponsors manage ePRO submissions from patients and sites with a central library that allows them to reuse ePROs across all their studies.

Sites manage participants and review ePRO data and adherence for improved communication with Sponsors.

Patients can access virtual visits, consent, and complete ePROs using MyVeeva for Patients. All data is captured and shared back to the sponsor’s central library for ongoing tracking.

Improve ePRO with a modern platform built for the unique needs of sponsors, sites, and patients.

Why Veeva ePRO

Build studies faster and smarter

  • Accelerate study design and execution

    Build, manage, and change studies faster with a modern designer and full reusability across studies.
  • Access high-quality data faster

    Ensure data is accurate, complete, and readily available from study design to close out.
  • Reduce site burden

    Simplify the setup, collection, and real-time review of ePROs for sites.
  • Improve patient experience

    Make ePRO completion easier with a single user-friendly app to access all study activities.


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Interested in learning more about how Veeva can help?