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.