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eCOA / ePRO

Facilitates real-time digital capture and storage of patient-reported outcomes, supporting multi-device use and multilingual data collection.

Solution by Cloudbyz
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Overview

The eCOA/ePRO solution by Cloudbyz is designed to enhance the patient experience by enabling electronic clinical outcome data capture with a focus on data quality and compliance. It integrates ePRO and eDiary functionalities to support the digital capture and storage of patient-reported outcome data, including data from wearable medical devices.

This solution is centered around patient-centricity, offering multi-gadget compatibility and supporting time-sensitive data collection in multiple languages. It also allows for the upload of multimedia content to improve patient education. Automated notifications and real-time alerts are provided to address any adverse events or deviations promptly.

The combination of ePRO and EDC offers a centralized view of clinical and patient-reported data, accelerating study build times and ensuring flexible workflows for both remote and on-site clinical trials.

Product Features

  • Visualize Data in Real-Time: Access real-time insights on patient-reported data through interactive dashboards and data visualization reports.
  • Participant Centric: Built on the Salesforce cloud platform, it offers ease of use and technical sophistication with a participant-centric approach.
  • Template Based: Utilizes templates for data setup, eliminating the need for programming, and providing ease of design and options for patients.
  • Interactive: Participants can navigate the patient diary checklist and questions step-by-step, ensuring structured and user-friendly navigation and submission.
  • API Enabled: Supports integration with IVR, clinical data systems, CTMS, and EDC through open APIs, enhancing productivity.
  • Multi-Device: Compatible with tablets, desktops, phones, and more, allowing study teams and patients to use their own devices.

Meta

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