Description
Clinion eSource is a modern, digital solution that empowers clinical trial participants to enter study-related data directly—under the supervision of site staff—eliminating the need for traditional paper handbooks. Fully integrated with Clinion EDC, it is part of the Clinion eCOA suite, designed to reduce data duplication, transcription errors, and missing entries.
With Clinion eSource, participants can enter their data during site visits, ensuring real-time accuracy and improving overall data quality.
Key Features:
Participant-Only Access: Only the subject/participant can enter and digitally sign their data. Investigators and CRCs have view-only access.
Real-Time Availability: Data entry becomes available after screening and informed consent is completed in Clinion EDC.
Digital Sign-Off: Participants must digitally sign their eCRF pages to submit data to the EDC.
Smart Validation: Missed data fields are highlighted, guiding participants to complete all required entries before submission.
Editable Window: Participants can edit their entries within 24 hours of submission. After that, entries are locked for integrity.
Seamless Integration: All submitted data flows directly into the Clinion EDC platform for further review and analysis.
Clinion eSource enhances participant engagement, ensures data integrity, and simplifies data collection in clinical trials.