Clinical TrialSoftware forConnected ClinicalResearch.
Connect data capture, consent, patient-reported outcomes, randomization, remote interactions and participant tracking in one operational framework.
KEY TAKEAWAYIn short: eTrialTrack is a unified eClinical platform — sponsors, CROs and research sites use it to run EDC, eConsent, ePRO, RTSM/IWRS, TeleHealth and participant tracking in one compliant system.
Watch raw trial data become decisions.
Every record from every source flows through the eTrialTrack engine — validated, checked and visualized in real time.
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.
How can one connected platform simplify clinical trial execution?
Clinical studies involve interconnected activities. Study teams configure the protocol, activate sites, enroll participants, collect clinical data, manage consent, capture participant-reported outcomes, coordinate treatment and supplies, support appropriate remote interactions and follow participants through study milestones. eTrialTrack brings these capabilities together as a modular technology framework so organizations can select the workflows relevant to their studies.
The platform is designed for sponsors, CROs, investigators, research sites, clinical operations teams and data management teams that need structured digital workflows without unnecessary fragmentation — with emphasis on practical configuration, data quality, operational visibility, traceability and connected study execution.
Why sponsors, CROs and biopharma choose eTrialTrack.
01Unified eClinical Platform
One integrated system for every trial activity — no more stitching together disconnected vendors and spreadsheets.
02Rapid Study Startup
Configure and deploy complex protocols in under three weeks with minimal implementation effort.
03Uncompromising Compliance
Built-in FDA 21 CFR Part 11, ICH-GCP, electronic signatures and immutable audit trails from day one.
04Real-Time Intelligence
Centralized dashboards surface enrollment trends, site performance and protocol deviations the moment they happen.
05Global Scalability
From a Phase I single-site study to a 100-site global program — the platform flexes to any trial size.
0624/7 Global Support
Dedicated clinical software engineers on call across every time zone your trial touches.
Tailored for clinical leaders.
eTrialTrack is designed for pharmaceutical and biotechnology organizations, CROs, research institutions, hospitals, investigators, research sites, clinical operations teams and data management teams evaluating digital clinical-trial workflows.
CRO
Multi-tenant study management, cross-sponsor visibility and operational speed that wins bids and delights sponsors.
Talk to a specialist
Global Pharma
Enterprise scalability, legacy system integration and always-on audit readiness across global development portfolios.
Talk to a specialistBiotech
Agile trial setup, lean budgets and decentralized trial capabilities that let breakthrough science move at startup speed.
Talk to a specialistClinical Research Technology Built Around the Study Journey
Our Journey. Our Purpose. Your Growth. — Since April 2024
Clinical studies involve interconnected activities. Study teams configure the protocol, activate sites, enroll participants, collect clinical data, manage consent, capture participant-reported outcomes, coordinate treatment and supplies, support appropriate remote interactions and follow participants through study milestones. eTrialTrack brings these capabilities together as a modular technology framework so organizations can select the workflows relevant to their studies.
The platform is designed for sponsors, CROs, investigators, research sites, clinical operations teams and data management teams that need structured digital workflows without unnecessary fragmentation. The emphasis is on practical configuration, data quality, operational visibility, traceability and connected study execution.
Designed for Practical Study Execution
eTrialTrack focuses on the questions research teams need to answer every day: Where is the data? What needs attention? Which participants have upcoming activities? What is the status of consent? Which queries remain open? What supplies are available? Which remote interactions are scheduled?
By organizing relevant information within defined workflows, eTrialTrack aims to help teams work with greater clarity while preserving the role of the protocol, investigator judgment, quality processes and applicable requirements.
Explore the eClinical platform
Who eTrialTrack clinical trial software is for
eTrialTrack is built for research organizations that want one compliant system for the full study workflow — here's exactly who uses it, what for, and when it pays off.
- Pharmaceutical and biotechnology sponsors running Phase I–IV programs
- CROs managing multi-sponsor, multi-study portfolios
- Research sites, hospitals and investigators digitizing study workflows
- Clinical operations and data management teams replacing spreadsheets
- End-to-end study execution: consent, data capture, patient-reported outcomes, randomization and remote visits
- Decentralized and hybrid trials with participants beyond the clinic
- Multi-site programs that need one real-time operational picture
- Inspection-ready studies requiring 21 CFR Part 11, GCP, HIPAA and GDPR alignment
- When your team stitches together disconnected tools and loses hours to reconciliation
- When an upcoming audit or inspection demands provable data integrity
- When study scale grows and manual tracking starts breaking down
Real feedback from real trial teams.
Verbatim answers and testimonials from our January 2026 client survey — shared anonymously, exactly as written.
"eTrialTrack has been a game-changer for our data management. The platform solved our ePRO integrity challenges through smart validation and a seamless user experience. We are now more efficient, query-free, and fully confident in our 21 CFR Part 11 compliance. A truly robust and reliable solution for modern clinical trials."
Regulatory armor, built in.
HIPAA
End-to-end PHI protection with AES-256 encryption at rest and in transit.
FDA 21 CFR Part 11
Certified electronic signatures, record integrity and full audit trails.
ICH-GCP
Good Clinical Practice standards embedded into every workflow.
GDPR
Data sovereignty controls and regional hosting for global trials.
ISO 27001
Security framework governing infrastructure, access and operations.
STANDARDS REFERENCESFDA 21 CFR Part 11ICH E6(R2) GCPGDPR
Designed for practical study execution.
eTrialTrack focuses on the questions research teams need to answer every day: Where is the data? What needs attention? Which participants have upcoming activities? What is the status of consent? Which queries remain open? What supplies are available? Which remote interactions are scheduled?
By organizing relevant information within defined workflows, eTrialTrack helps teams work with greater clarity while preserving the role of the protocol, investigator judgment, quality processes and applicable requirements.
Go Live in Weeks
Industry average eClinical setup is 4–6 months. eTrialTrack deploys complex protocols in under three weeks.
Platform, Zero Sprawl
EDC, eConsent, ePRO, RTSM, Telehealth and tracking in one system — replacing 5+ disconnected vendor tools.
Audits, Zero Findings
Every client audit passed without a single critical finding — compliance is engineered in, not bolted on.
Humans, Always On
Real clinical software engineers on call in every timezone your trial touches — not a ticket queue.
What exactly is eTrialTrack?
eTrialTrack is a unified eClinical platform that manages clinical trials end to end. It combines EDC, CTMS, eConsent, ePRO, RTSM/IWRS, Telehealth and participant tracking in one secure system — replacing a patchwork of disconnected vendors.
How long does it take to launch a study?
Most studies are configured and deployed in under three weeks. Our no-code CRF builder and reusable protocol libraries eliminate the long programming cycles typical of legacy EDC systems.
Is the platform compliant with FDA and global regulations?
Yes. eTrialTrack supports FDA 21 CFR Part 11, ICH-GCP, HIPAA and GDPR requirements out of the box — including electronic signatures, immutable audit trails and role-based access controls. We have passed 40+ client audits.
Can eTrialTrack run decentralized or hybrid trials?
Absolutely. Integrated Telehealth, eConsent, ePRO and participant tracking let patients complete study activities remotely while sponsors maintain data quality and regulatory compliance.
Does it integrate with our existing systems?
Yes. The platform offers standard APIs and supports regulatory-ready data formats (CDISC SDTM) for smooth integration with safety systems, labs, and downstream analytics pipelines.
Who is eTrialTrack built for?
Sponsors, Contract Research Organizations, biotech companies, pharmaceutical organizations, academic research institutions and clinical sites looking for scalable clinical trial software.
Is clinical trial software compliant with FDA regulations?
Yes, modern clinical trial software must comply with stringent global regulations including FDA 21 CFR Part standards. Trusted platforms integrate built-in audit trails, secure electronic data capture, and certified frameworks to ensure total data integrity, seamless inspection readiness, and uncompromising compliance throughout every phase of research.
Two ways to start.
Book a live demo call and get a calendar invite instantly — or grab a module brochure straight to your inbox.