VEEVA ePRO

High-Quality Patient Data
When You Need It, Where You Need It

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

Announced 2022
Status EARLY
Customers 1-10

Veeva ePRO (electronic Patient Reported Outcomes) captures questionnaire responses directly from clinical trial patients using an app or webpage.

Sponsors manage the ePROs through their own interface, and a central library allows them to reuse ePROs across all their studies.

Sites have a simple access point to manage their participants and can review ePRO data and adherence.

Patients complete the ePRO using MyVeeva for Patients (native application or web), where they can also access other activities like consent or virtual visits. Once complete, the data flows back into the sponsor’s environment.

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.
  • Improve patient experience

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

RESOURCES

Explore and learn

A new approach to de-risk your ePRO strategy
View webinar
Make taking part in a clinical trial more accessible and convenient
Watch demo
Get high-quality patient data when you need it, where you need it
Download features brief

Interested in learning more about how Veeva can help?