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