Enable Patient-centric,
Paperless Clinical Trials

Gain efficiencies and deliver a better experience
through connected patient solutions.

Enhance Patient Engagement

Make trial participation easier for patients, and streamline study execution for research sites and trial sponsors.

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Improve the Research Experience

Keep patients informed and connected
through a single application for all their
clinical trial activities.

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Reduce Site Burden

Make study execution easier for sites by providing an easy-to-use solution to manage patient interactions across all studies.

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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.

eConsent

eConsent

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.

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ePRO

ePRO

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 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.

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Resources

Shifting from Paper to Digital Patient Consent
Article Shifting from Paper to Digital Patient Consent
Veeva Digital Clinical Trials Survey Report
Report Veeva Digital Clinical Trials Survey Report
Drive Paperless, Patient-centric Trials with MyVeeva
Webinar Drive Paperless, Patient-centric Trials with MyVeeva
Perspectives on Moving Toward Paperless, Patient-centric Trials
White Paper Perspectives on Moving Toward Paperless, Patient-centric Trials