eTrialTrack TeleHealth is designed as a study-enablement component for protocols that permit remote interactions. It can support scheduled video consultations and participant interactions while connecting relevant information to the broader study workflow.
eTrialTrack TeleHealth is designed as a study-enablement component for protocols that permit remote interactions. It can support scheduled video consultations and participant interactions while connecting relevant information to the broader study workflow.
Supports Appropriate Remote Workflows. eTrialTrack focuses on supports appropriate remote workflows as part of a practical study workflow.
Participant Convenience. eTrialTrack focuses on participant convenience as part of a practical study workflow.
Connected Participant Journey. eTrialTrack focuses on connected participant journey as part of a practical study workflow.
Operational Visibility. eTrialTrack focuses on operational visibility as part of a practical study workflow.
Protocol-Aware Approach. eTrialTrack focuses on protocol-aware approach as part of a practical study workflow.
Where appropriate, TeleHealth 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 TeleHealth 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 TeleHealth is designed as a study-enablement component for protocols that permit remote interactions. It can support scheduled video consultations and participant interactions while connecting relevant information to the broader study workflow.
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.