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Live Webinar | Challenges & Solutions: Designing ePRO and eConsent for Pediatric Trials
Wednesday, July 24th 
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Power meets user-centricity with Curebase EDC.

Seamlessly integrated with Curebase’s ePRO/eCOA suite, our EDC enables hybrid and site-based studies that users will love and that streamline all of your data collection into a single, modern experience.

Trusted by Industry-Leading Teams

Trusted by
250K
participants
30K
consents signed
8.4M
data points collected
83
studies Powered
intuitive forms

Reduce site burden with forms that are easy, intuitive, and highly configurable.

Data entry can be simple with user-centric design. Experience elegant direct data capture of CRF entry, log forms, adverse event and medication reporting, helpful dashboards for PI sign off, notifications, reminders, and more. Delightful experience on laptops and tablets.

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manage data Curebase platform

Review and manage data in a system built with user experience in mind.

Issue queries, freeze and lock data, manage your case report exports, complete data review workflows, and more while reducing site burden and giving users an experience they will love.

Curebase platform ePRO

Stay on top of your study with the powerful reporting needed to run a study at scale.

Getting insight should be simple. Empower sites to stay on top of every patient’s status in the study and leverage powerful in-appnotifications and communication.

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EDC is just the foundation. Combine it with ePRO/eCOA and eConsent for a seamless experience.

Curebase platform  ePro eCOA
embed forms Curebase platform
eConsent Curebase platform
payment integrations Curebase platform

Launch your study faster

Curebase's study designer enables complex builds, optimized for every step of the participant experience. Choose self-service or go fully-outsourced—it's your call.

Curebase platform  Study Designer
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