Clinion EDC

This feature is purpose-built to safely and rapidly import various data from multiple external sources directly into the system. Data transfer occurs directly from external files into the platform via one fluid batch process. Following the import, the system autonomously initiates the process to run batch edit checks on the newly added data set.

The administrative module oversees the complete set of operational tasks throughout the clinical trial. This oversight encompasses the management of all associated sites, personnel accounts, and defined access roles within the system platform. Furthermore, the module governs the organization of medical dictionaries, thus ensuring standardization across the entire study.

ECRF Configuration allows for the direct selection of customizable forms from the Global Library to accelerate study initialization. New Electronic Case Report Forms (eCRFs) are also generated via a straightforward, no-code drag-and-drop feature. The system implements AI CDASH coding to autonomously annotate all data fields in accordance with mandated CDISC standards.

The scheduler accurately plans and organizes all study visits for every single enrolled subject with speed. It tracks the comprehensive visit timeline, commencing from the initial enrollment and concluding at the designated final visit. Furthermore, this module autonomously records and tracks any observed protocol deviations throughout the study.

Clinion EDC software facilitates the necessary setup of both local and global laboratory facilities for each distinct study site. Full control is provided to manage the diverse laboratory reference ranges across all Case Report Forms (CRFs). This key capability is essential for ensuring all laboratory data is standardized and meets quality expectations.