Staci McDonald, Vice President Global Scientific Clinical Operations, Celerion Discusses the Power of Digital Trials:

Patient-Centric

Easier to share information with participants and collect data remotely, where possible

Faster Access to Data

Data only needs to be entered once, then it proliferates throughout the rest of the system

Always Inspection-Ready

Information is readily available to sites, sponsors, and monitors in real-time

“The continuity of having information at your fingertips and being able to answer questions instantly is invaluable”
Staci McDonald,
Vice President Global Scientific Clinical Operations, Celerion
econsent-case-study

eConsent Case Study

Learn how Celerion increased efficiencies across the consenting process

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Veeva-Site-Connect

Veeva Site Connect

Streamline information sharing for better collaboration and faster trials

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Veeva-Site-Connect

Veeva ePRO

Simplify the design, management, and completion of electronic Patient Reported Outcomes

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Resources

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Video Celerion and Veeva Partnering in Digital Trials
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