Clinical Data

Veeva eCOA

Take eCOA off your
critical path

Modern solution to simplify the design, management, and completion of eCOA for sponsors, sites, and patients.

Announced 2022 Status Early Customers 11-50
Veeva eCOA | Simplify eCOA Delivery and Management
6 new standards to simplify eCOA delivery and management
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Overview

Fast, easy, connected

Veeva eCOA (electronic Clinical Outcome Assessments) captures questionnaire responses directly from clinical trial patients (ePRO), clinicians (eClinRO), or patient caregivers (eObsRO) using an app or webpage.

Sponsors manage the eCOAs through their own interface, and a central library allows them to reuse eCOAs across all their studies. See list of validated instruments.

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

Patients and caregivers complete the questionnaires 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 eCOA

Build studies faster and smarter