iMednet ePRO

iMednet ePRO is an electronic patient-reported outcomes module built natively within the iMednet eClinical platform by Mednet. Designed to meet the growing demands of virtual participation and patient engagement in clinical trials, it streamlines onsite and offsite data capture for both study participants and research coordinators. Optimized for mobile devices and accessible anytime, anywhere, iMednet ePRO is suited for research sponsors and CRO partners seeking a cost-effective, integrated solution for modern study designs.

As a native module within the broader iMednet eClinical platform, iMednet ePRO integrates seamlessly with EDC, RTSM, eConsent, Adjudication, Payments, DICOM Imaging, and other tools, enabling a unified approach to clinical trial management across all study types and phases.

Questionnaire Design and Customization

• Supports both standard instrument templates and highly customized questionnaires.
• Accommodates commonly used form templates such as Euroqol EQ-5D.
• Streamlines the process for study designers to build and configure ePRO questionnaires efficiently.

Site User and Coordinator Experience

• Functions as a seamless extension of iMednet EDC, allowing site users to navigate directly to the ePRO module.
• Accessible on tablet and mobile devices for flexible administration.
• Customized columns in the ePRO list can display variables such as date of birth, patient ID, email address, or other identifiers to help research team members quickly identify the correct study participant.
• Enables coordinators to assign appropriate questionnaires to the right participants with ease.

Participant-Facing Features

• Designed to be highly intuitive and easy to use for study participants.
• Accessible and optimized for any tablet or mobile device without requiring participants to download a dedicated app.
• Features a simple, modern interface with a tile format, swipe navigation, and visual cues and prompts to guide participants through next steps.
• System reminders alert participants when questionnaire due dates are approaching.

Reporting and Study Oversight

• Provides real-time reports and status tracking of patient-reported outcomes at any time.
• Intuitive dashboards offer visibility into the number of questionnaires assigned and their completion status.
• Reporting is available at the study, site, and participant level for comprehensive oversight.

iMednet ePRO is part of Mednet's comprehensive EDC-centric eClinical platform, which supports all study types and phases. The platform's native, fully integrated suite of modules is designed to simplify study build times, increase execution efficiency, and minimize costs throughout the duration of a clinical trial.