eTrialTrackOne Clinical Workflow, Six Connected Capabilities
Choose the modules that fit your study and connect them around the participant, site and data workflows that matter most.
Every trial requirement. One command center.
Electronic Data Capture provides a structured environment for clinical data. eConsent supports digital consent workflows. ePRO enables protocol-defined patient-reported data collection. RTSM/IWRS supports randomization and trial supply operations. TeleHealth supports appropriate remote interactions. Participant Tracker provides an operational view of participant progress and milestones.
Each capability can be evaluated independently or connected where the study requires a broader participant, site and data workflow.
Serving clinical research teams in Mumbai, Hyderabad, Ahmedabad, Pune and Delhi — with deployments across 24 countries.
Electronic Data Capture
eTrialTrack EDC provides a structured digital environment for sponsors, CROs, investigators and research sites that need consistent electronic clinical data capture. The focus is on configurable forms, validation, query management, traceability, reporting and connected workflows.
Deployed standalone or as part of the full unified suite — your call.
Electronic Data Capture
EDC provides a structured environment for configuring eCRFs, applying validation rules, managing queries, reviewing data and reporting study activity.
Electronic Consent
eConsent supports digital consent workflows including controlled content, version management, signatures, consent status and re-consent where appropriate.
Electronic Patient-Reported Outcomes
ePRO supports protocol-defined questionnaires, scheduled assessments, reminders, validation and participant-reported data workflows.
RTSM / IWRS
RTSM/IWRS supports randomization, treatment assignment, eligibility rules, inventory and trial supply workflows.
TeleHealth
TeleHealth supports appropriate remote interactions, scheduled video consultations and connected participant workflows where the protocol permits.
Participant Tracker
Participant Tracker provides an operational view of enrollment, visits, milestones, follow-up and participant-level progress.
How the Capabilities Work Together
A study can use one product or connect multiple capabilities. For example, participant enrollment may lead into consent, data capture, patient-reported assessments, scheduled interactions and follow-up. The exact configuration should be determined by study requirements and supported integrations.
Implementation Approach
Start with study requirements, map the workflow, select relevant capabilities, configure the system, connect supported integrations and provide appropriate implementation and support.
Who our clinical trial solutions are for
Six connected capabilities, one platform — adopt the module your study needs today and connect the rest when the workflow demands it.
- Data management teams (EDC), regulatory and site staff (eConsent)
- Outcomes researchers and coordinators (ePRO), supply and randomization teams (RTSM/IWRS)
- Decentralized trial teams (TeleHealth), recruitment and retention teams (Participant Tracker)
- Sponsors and CROs who want all of the above in one tenant
- Single-module adoption — e.g. start with EDC for one study
- Connected workflows: enrollment → consent → capture → outcomes → randomization → remote visits
- Portfolio standardization across sponsors, studies and sites
- When a new study needs to start in weeks, not months (2–4 week typical deployment)
- When per-vendor contracts and integrations are slowing your team down
- When leadership wants one audit-ready compliance posture across every module
Frequently asked questions
What products does the eTrialTrack platform include?
Six connected capabilities: Electronic Data Capture (EDC), electronic consent (eConsent), electronic patient-reported outcomes (ePRO), RTSM/IWRS randomization and trial supply, TeleHealth video consultations and a participant tracker.
Can we adopt one module first and add more later?
Yes. Each capability can be evaluated and deployed independently, then connected to others when the study requires a broader participant, site and data workflow.
How do the modules work together in a study?
A study can connect enrollment to consent, data capture, patient-reported outcomes, randomization and remote visits, so teams work from one operational picture instead of disconnected tools.
How long does implementation take?
Standard tenant provisioning completes within 3-5 business days of contract signing; study-specific configuration timelines are confirmed in your statement of work.