You control the eCRF, not the other way around. Design and customise based on your unique medical device study needs.
Ensure high quality data capture for your clinical investigation
Choose from 17 different ready to use auto-validated question types
eCRF's for simple or complex protocols with no limits
Create links with Module References to other Study modules such as Unscheduled Events, Adverse Events module and Concomitant Medications. Create new entries directly from the eCRF
Set up advanced validation rules on individual questions. Trigger SMART-TRIAL to automatically show a warning message, create a query, or block the data input.
Ready-to-use MDR and ISO 14155:2020 AE teamplate with automatic rules and notifications.