Unified eClinical Platform. Smarter Clinical Trials
Clinical Trial Management Software Built to Accelerate Research
eTrialTrack is a unified eClinical software platform that combines Electronic Data Capture (EDC), Clinical Trial Management Software (CTMS), eConsent Software, RTSM/IWRS, ePRO Software, Telehealth, and patient engagement tools into one secure, FDA-compliant solution for sponsors, CROs, biotech, and pharmaceutical companies.
Revolutionizing Clinical Research with Innovation
Quantum delivers advanced eClinical platform solutions designed to enhance efficiency, accelerate clinical trials, and enable smarter, data-driven decision-making.
Our Journey. Our Purpose. Your Growth.
Delivering excellence through experience, scale, and trust.
10
Lakh+Patient Cases Handled
40+
AuditsClient Audits Completed
15
Lakh+Clinical Hours Invested
10
Lakh+Patient Case Records Created
15+
YearsExperience with EDC Systems
Electronic Data Capture (EDC) Software for Clinical Trials
eConsent Software for Digital Clinical Trial Consent
Electronic Patient-Reported Outcomes (ePRO) Software
eSource Software for Electronic Clinical Data Capture
eTMF Software for Clinical Trial Document Management
RTSM Software for Clinical Trial Randomization & Supply
Unified eClinical Research Software for Modern Clinical Trials
eTrialTrack is a comprehensive clinical research software platform designed to streamline data capture, patient engagement, study management, and regulatory compliance throughout the clinical trial lifecycle.
eTrialTrack Features
Real-Time Data Entry & Access
Investigators and study teams can enter data directly at the point of capture, enabling immediate validation, faster data reviews, and more timely decisions.
Enhanced Data Accuracy & Compliance
With built-in edit checks, audit trails, and role-based access controls, eTRIALTRACK helps ensure that data is clean and fully compliant with regulatory frameworks like FDA 21 CFR Part 11 and ICH-GCP.
Streamlined Study Design
eTrialTrack platforrn offer intuitive CRF (Case Report Form) builders, allowing study teams to design and deploy study forms rapidly without the need for extensive programming.
Scalability & Flexibility
Whether for early-phase trials or large-scale global studies, eTrialTrack can be tailored to meet the needs of of a wide range of therapeutic areas and study protocols.
Improved Monitoring & oversight
Sponsors and CROs gain better visibiliiy into trial progress, enrollment, data trends, and site performance with real-time dashboards and automated reporting.
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Selecting the right EDC platform drives up to 89% of effective data management throughout the trial lifecycle, resulting in lower operational costs, streamlined workflows and faster, more confident decision-making.
Providing integrated solutions that enhance operational efficiency, collaboration, and visibility across clinical trial management processes and workflows.
Global Pharma is transforming healthcare by delivering innovative and reliable pharmaceutical solutions worldwide.
The biotech industry drives scientific breakthroughs that improve patient care and global health outcomes.
Why Sponsors, CROs, and Biopharma Companies Choose eTrialTrack
eTrialTrack delivers a complete clinical research platform built to reduce operational complexity, improve compliance, and accelerate clinical development.
Unified eClinical Platform
Faster Study Startup
Regulatory Compliance
Real-Time Reporting & Analytics
Scalable for Any Trial Size
24/7 Global Support
Frequently Asked Questions
Our Frequently Asked Questions section addresses the most common technical and operational queries about our Clinical Trial Application software. From compliance and integrations to submission workflows and data security, these answers are designed to help sponsors, CROs, and sites better understand how the platform simplifies regulatory submissions and ensures smooth trial operations.
Detailed FAQs section refer to FAQ page on the website or write to us on info@quantum-quip.com
What is eTrialTrack?
eTrialTrack is a unified eClinical platform that helps sponsors, CROs, biotech, and pharmaceutical companies manage clinical trials from start to finish. The platform combines Electronic Data Capture (EDC), Clinical Trial Management Software (CTMS), eConsent, ePRO, RTSM, Telehealth, and participant tracking in one secure system.
What is a Unified eClinical Platform?
A unified eClinical platform brings together all the essential tools needed to run a clinical trial, including EDC software, CTMS software, eConsent, ePRO, and RTSM. Instead of using multiple disconnected systems, research teams can manage study operations, patient data, and compliance from a single platform.
What is Electronic Data Capture (EDC) Software?
Electronic Data Capture (EDC) software is used to collect, validate, and manage clinical trial data electronically. Compared to paper-based processes, EDC software for clinical trials improves data accuracy, reduces manual errors, and enables faster study monitoring and reporting.
How does Clinical Trial Management Software (CTMS) help research teams?
Clinical Trial Management Software (CTMS) helps sponsors and CROs manage study planning, site performance, participant enrollment, monitoring activities, and regulatory documentation. A modern CTMS platform improves operational efficiency and provides better visibility across the entire clinical trial lifecycle.
Is eTrialTrack compliant with FDA and global regulatory requirements?
Yes. eTrialTrack is designed to support FDA 21 CFR Part 11 compliance, ICH-GCP guidelines, audit trails, electronic signatures, and role-based access controls. These features help organizations maintain compliance while ensuring secure and reliable clinical trial data management.
What is eConsent in clinical trials?
eConsent software allows participants to review study information and provide informed consent electronically. By digitizing the consent process, electronic informed consent improves participant understanding, simplifies documentation, and enhances compliance in clinical research studies.
What is ePRO software and why is it important?
ePRO software (Electronic Patient Reported Outcomes) enables participants to submit symptoms, treatment experiences, and health-related information through mobile devices or web applications. This helps research teams collect real-time patient data and improve participant engagement throughout the study.
What is RTSM software?
RTSM software (Randomization and Trial Supply Management) automates patient randomization, treatment assignment, and clinical supply management. By using RTSM/IWRS software, study teams can reduce errors, improve drug accountability, and maintain protocol compliance across multiple study sites.
Can eTrialTrack support decentralized clinical trials?
Yes. eTrialTrack supports decentralized clinical trials (DCTs) through integrated Telehealth, eConsent, ePRO, and participant engagement tools. These capabilities allow participants to complete study activities remotely while helping sponsors maintain data quality and regulatory compliance.
Who can use eTrialTrack?
eTrialTrack is designed for sponsors, Contract Research Organizations (CROs), biotechnology companies, pharmaceutical organizations, academic research institutions, and clinical research teams looking for a scalable clinical trial management software solution.
