ePRO is a Low Cost Solution to Capture Real-Time
Patient Data.

Automatically Integrate Patient Submitted Data With Your Clinical Trial Software.

Electronic Patient Reported Outcome (ePRO) helps sponsors and CROs capture more complete patient data that can be used to speed up trials and improve marketing efforts post drug and device approval.


Key Benefits  of Implementing ePRO for Clinical Trials

  • Reduces clinical trial risk by capturing more patient data on devices. This mitigates regulatory risk, patient compliance, and adverse events.
  • Accelerates timelines by reducing manual data entry and data clean up. Real-time data provides faster insights and less statistical variance.
  • Helps senior management make better, faster decisions by giving them real-time data and alerts to
    alleviate trial issues.
  • Lowers costs of clinical trial from paper resources, personnel costs, lab costs, and more.

ePRO Automation Improves Efficiency and Decreases Mistakes of Manual Processes.

  • Collects information via smartphone that is automatically integrated into IRT
  • Integrates real-time, leading to faster insights and decision making
  • Enables instant alerts from trial site to patient’s ePro device, improving patient retention
  • Increases efficiency and reduces costs

About the Trialogics ePRO Application and Device

The Trialogics ePRO application is deployed utilizing an Android smartphone. The smartphone is supplied to the patient via the clinical trial site.

The ePRO device:

  • Controlled 100% by Trialogics
  • Can be used to connect to other devices such as wearables and mobile health sensors
  • Automatically syncs data with clinical trial IRT systems

Inside the ePRO Device

The Trialogics ePRO software includes:

  • Patient questionnaires and alerts
    to prompt compliance
  • Calendar to help improve patient retention
  • Site contact information

The Demand for ePRO is Increasing

The FDA is demanding increasing patient perspective during the course of clinical trials. ePRO answers this demand by placing the power of data collection in the patient’s hands.

A smartphone app with patient diaries, alerts, and wearable connection collects data and integrates with your clinical trial software.

ePro Can Integrate With IRT System or Be Used Separately

Whether you choose to use ePRO in tandem with your IRT software or implement it as a separate tool, ePRO’s integration into your trial is seamless.

100% Data Security

The data collected is 100% secured and encrypted and is transmitted to the appropriate Trialogics database for the specific clinical trial.

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