Once programmed to meet the needs of your specific trial requirements, the Clinical eSource Platform eliminates the guesswork from running all phases of clinical trials by fully automating each step within your workflow with meticulous precision and accuracy.
Whether you choose to fully automate your clinical trial—or choose to integrate real-time bi-directional data exchange to augment your current EDC solution—the Clinical eSource Platform allows you to harness the power of a truly paperless eSource solution.
The Clinical eSource Platform captures and analyzes data at the edge with enhanced speed and accuracy across all phases of clinical trials. Its unique ability to accommodate any connected device irrespective of its modality enables real-time bi-directional data exchange of the highest quality–in a true eSource solution that is 100% paperless.
The Clinical eSource Platform eliminates the need for paper across clinical trials of all phases by seamlessly introducing connectivity and automation. By reducing the demands put on participants and clinical researchers, protocol adherence is maximized—resulting in higher quality, real-time data collection.
The Clinical eSource Platform is powered by intricate layers of granular data that drive and capture step-by-step processes for study coordinators, principal investigators, other site personnel, and CRAs, providing superior transparency and oversight that enhances inspection readiness.
