eCaseLink eConsent

eCaseLink eConsent is a participant data capture tool designed for use in clinical trials. It can be deployed as a standalone application or as part of the eCaseLink EDC platform, supporting both on-site and remote data collection via any web-connected device, including smartphones, tablets, laptops, and desktops.

The tool is built around a patient-centric design that allows participants to review study documentation and provide electronic signature consent. It is intended for use in a range of settings, including operating rooms, clinics, doctor's offices, and fully remote environments, recording participant consent with accurate time, date, and signature data alongside investigator signature to reduce the risk of review findings.

Key Features

• Supports real-time data collection and TeleHealth use cases
• Built-in eSignature functionality for both participant and investigator
• Presents study information in written, visual, and audio-visual formats to support participant understanding
• Supports interactive videos and other validated assessment tools
• Promotes remote monitoring to improve data quality and participant engagement
• Accessible on any web-connected device, including smartphones, iPads, mini tablets, laptops, and desktops

Deployment and Integration

• Can be used as a standalone informed consent tool or integrated within the eCaseLink EDC platform
• When used with eCaseLink EDC, supports combined reporting and data analysis workflows
• Provides a secure, responsive interface suitable for both on-site and off-site data capture scenarios

eCaseLink eConsent is designed to replace paper-based linear consent processes with a multimedia approach, aiming to improve the accuracy of consent records and the quality of participant engagement throughout a clinical trial.