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Solutions

Electronic Patient-Reported Outcomes Software.

KEY TAKEAWAY

eTrialTrack ePRO is designed to allow participants to provide protocol-defined information through digital workflows. It can support scheduled assessments, reminders, validation and synchronization with relevant clinical data workflows.

ePRO • ENGAGEMENT

What you get

Mobile, Tablet and Web Access
Protocol-Defined Questionnaires
Scheduled Assessments
Participant Reminders
Data Validation
Multilingual Workflows
Data Synchronization
Completion Visibility
DIARY COMPLIANCE RATE
94%
Average across active customer deployments

What Is eTrialTrack ePRO?

eTrialTrack ePRO is designed to allow participants to provide protocol-defined information through digital workflows. It can support scheduled assessments, reminders, validation and synchronization with relevant clinical data workflows.

Why Choose eTrialTrack ePRO?

Direct Participant Data Capture. eTrialTrack focuses on direct participant data capture as part of a practical study workflow.

Structured Assessments. eTrialTrack focuses on structured assessments as part of a practical study workflow.

Connected Study Operations. eTrialTrack focuses on connected study operations as part of a practical study workflow.

Operational Visibility. eTrialTrack focuses on operational visibility as part of a practical study workflow.

Designed Around the Protocol. eTrialTrack focuses on designed around the protocol as part of a practical study workflow.

How It Fits the Broader Study Workflow

Where appropriate, ePRO can be connected with other eTrialTrack capabilities to support a more coherent participant, site and data workflow. The exact configuration should follow the study protocol, organizational procedures, supported integrations and agreed implementation scope.

AUDIENCE & USE CASES

Who eTrialTrack ePRO is for

The ePRO module serves specific roles in a study team — here's who uses it, the use cases it supports, and when your study needs it.

WHO IT'S FOR
  • Outcomes researchers collecting patient-reported endpoints
  • Study coordinators managing instrument schedules
  • Participants reporting symptoms and quality of life from home
USE CASES IT SUPPORTS
  • BYOD eDiaries and symptom tracking with automated reminders
  • Validated QoL and efficacy instruments, multilingual delivery
  • Real-time adherence monitoring and missing-data prevention
WHEN YOU NEED IT
  • When paper diaries come back incomplete or back-filled
  • When endpoint quality depends on timely, in-the-moment reporting
  • When you need adherence visibility before the next site visit
FAQS

Frequently asked questions

What is eTrialTrack ePRO?

eTrialTrack ePRO is designed to allow participants to provide protocol-defined information through digital workflows. It can support scheduled assessments, reminders, validation and synchronization with relevant clinical data workflows.

Is the ePRO module compliant for regulated clinical trials?

Yes. eTrialTrack is designed around FDA 21 CFR Part 11, ICH-GCP, HIPAA and GDPR expectations, with electronic signatures, complete audit trails and role-based access controls.

How quickly can our team deploy the ePRO module?

Most teams go live in two to four weeks, including configuration, validation support and role-based training for coordinators, data managers and monitors.

Can we see ePRO in a live demo?

Yes. Book a 30-minute guided walkthrough and the team will tailor it to your study setup, workflows and protocol requirements.