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iMednet ePRO

Streamlines electronic patient-reported outcomes collection for clinical trials, optimized for mobile use, enabling easy data capture and questionnaire creation.

Solution by Mednet
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Overview

iMednet ePRO simplifies the collection of electronic patient-reported outcomes (ePRO) for clinical trials, addressing the growing need for virtual participation and patient engagement. This module facilitates both onsite and offsite data capture, making it accessible and straightforward for study participants and research coordinators. Optimized for mobile devices, it allows intuitive entry of study-related information anytime, anywhere.

Easily create standard or customized questionnaires

The iMednet ePRO module, integrated within a comprehensive platform, enables study designers to efficiently build ePRO questionnaires. It supports standard instruments like Euroqol EQ-5D and allows for the creation of highly customized questionnaires.

Highly intuitive and easy to administer

Site users can seamlessly access the ePRO module on tablets or mobile devices. The module's customizable columns can include variables such as date of birth, patient ID, and email address, aiding research team members in identifying study participants and assigning questionnaires.

Accessible and easy for study participants

Designed as an end-to-end solution, iMednet ePRO is user-friendly for study participants. It is accessible on any tablet or mobile device without requiring a unique app download. The interface features a simple, modern design with tile format, swipe navigation, and visual cues, making it easy for participants to understand their next steps. System reminders notify participants of approaching due dates.

Track status and easily access real-time reports

Within the iMednet platform, research teams can access real-time reports and the status of PROs at any time. Intuitive dashboards and reports offer visibility into the number of questionnaires assigned and their completion status at the study, site, and participant levels.

Contact Mednet for more information about their comprehensive EDC-centric eClinical platform, which includes key native modules for various study types and phases, such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent, and more.

Meta

Category
Clinical Trial Management
Field(s)
Clinical & Trials
Target user(s)
Clinical / Diagnostic Professional
Tag(s)
Clinical Trials Management