Enhance Patient Engagement
Make trial participation easier for patients, and streamline study execution for research sites and trial sponsors.
Improve the Research Experience
Keep patients informed and connected
through a single application for all their
clinical trial activities.
Reduce Site Burden
Make study execution easier for sites by providing an easy-to-use solution to manage patient interactions across all studies.
Streamline Study Execution
Get studies up and running faster and streamline end-to-end management of patient engagement solutions through a connected digital trial platform.
Veeva eConsent simplifies the set-up, completion, and review of informed consent through an end-to-end process that reduces administrative burden and delivers a better experience for sites and patients.Learn more
Veeva ePRO increases efficiencies through integrated workflows that enable end-to-end management of ePRO solutions from creation through data capture to reporting.Coming soon
MyVeeva for Patients App
MyVeeva for Patients is a simple, intuitive application that makes trial participation more accessible and convenient for patients. With a single point of access for clinical trial documents, actions, and communications, patients can easily view study information and stay in touch with their clinical site.Learn more