Capture, manage, and report clinical research data

Build forms in minutes and collect data accurately with form rules such as edit checks and skip logic.
EDC - Collect clinical trial data, build case report forms, CRFs, and manage queries.

Peace of mind for regulatory submission

From ICH/GCP and 21 CFR to GDPR and HIPAA, we provide you the tools to focus on the trial with complete.

Fast and easy mid-study changes

Change, validate, and deploy mid-study changes without tech support or taking your study offline. Conveniently make modifications at no additional cost.

Get clean data faster

Drive efficiency in data cleaning and improve time to database lock with a flexible, formless view of your data that is optimized for monitoring and review.

Build CRFs in few clicks

Design and Build Studies Faster

Build your visit schedules, case report forms, edit checks and workflows rapidly. Quickly progress from design to user acceptance testing to First Patient In across all your sites.

Manage clinical trial participants directly in the EDC

Access to the data you need

Fast and intuitive interface for capturing and reviewing clinical trial data. View the data that requires your attention first to accelerate timeline and increase safety.

Manage clinical trial queries directly in the EDC

In-form query resolution

Issue and reply to queries from within the system for faster turnaround. In-form query resolution improves data accuracy

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A tour of Zapclinica just for you - how it works, and how it can meet your needs.

Part of the Zapclinica platform

Zapclinica helps you managing your clinical trial, reduces the time to market, the cost, and the burden to run a successful clinical trial by operationally streamlining every task in an all-in-one platform.

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