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”
eConsent Case Study
Learn how Celerion increased efficiencies across the consenting process
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Streamline information sharing for better collaboration and faster trials
Learn MoreVeeva ePRO
Simplify the design, management, and completion of electronic Patient Reported Outcomes
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