eTrialTrack RTSM/IWRS supports controlled randomization and trial supply workflows through a structured digital environment. The system can bring together treatment assignment, inventory visibility, site access, eligibility rules, kit tracking and relevant audit information.
eTrialTrack RTSM/IWRS supports controlled randomization and trial supply workflows through a structured digital environment. The system can bring together treatment assignment, inventory visibility, site access, eligibility rules, kit tracking and relevant audit information.
One Controlled Workflow. eTrialTrack focuses on one controlled workflow as part of a practical study workflow.
Study-Specific Configuration. eTrialTrack focuses on study-specific configuration as part of a practical study workflow.
Operational Visibility. eTrialTrack focuses on operational visibility as part of a practical study workflow.
Reduced Reconciliation. eTrialTrack focuses on reduced reconciliation as part of a practical study workflow.
Connected Clinical Platform. eTrialTrack focuses on connected clinical platform as part of a practical study workflow.
Where appropriate, RTSM/IWRS 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 RTSM/IWRS 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 RTSM/IWRS supports controlled randomization and trial supply workflows through a structured digital environment. The system can bring together treatment assignment, inventory visibility, site access, eligibility rules, kit tracking and relevant audit information.
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.