eTrialTrack Participant Tracker provides an organized participant-level operational view across screening, enrollment, visits, follow-up and study milestones. The focus is operational visibility rather than clinical decision-making.
eTrialTrack Participant Tracker provides an organized participant-level operational view across screening, enrollment, visits, follow-up and study milestones. The focus is operational visibility rather than clinical decision-making.
A Clear Participant Journey. eTrialTrack focuses on a clear participant journey as part of a practical study workflow.
Earlier Operational Visibility. eTrialTrack focuses on earlier operational visibility as part of a practical study workflow.
Connected Workflows. eTrialTrack focuses on connected workflows as part of a practical study workflow.
Reduced Manual Tracking. eTrialTrack focuses on reduced manual tracking as part of a practical study workflow.
Operational Rather Than Clinical. eTrialTrack focuses on operational rather than clinical as part of a practical study workflow.
Where appropriate, Participant Tracker 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.
The Participant Tracker module serves specific roles in a study team — here's who uses it, the use cases it supports, and when your study needs it.
eTrialTrack Participant Tracker provides an organized participant-level operational view across screening, enrollment, visits, follow-up and study milestones. The focus is operational visibility rather than clinical decision-making.
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.
Most teams go live in two to four weeks, including configuration, validation support and role-based training for coordinators, data managers and monitors.
Yes. Book a 30-minute guided walkthrough and the team will tailor it to your study setup, workflows and protocol requirements.