Unified eClinical Platform

Unified eClinical Platform. Smarter Clinical Trials

Clinical Trial Management Software Built to Accelerate Research

eTrialTrack is a unified eClinical platform that combines Electronic Data Capture (EDC), CTMS software, eConsent, RTSM/IWRS, ePRO, Telehealth, and patient engagement tools into one secure, compliant solution.

Compliance
21 CFR Part 11
Accuracy
99.9%
Clinical Innovation

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.

Studies
120+
Countries
24

Our Journey. Our Purpose. Your Growth.

20+
Years Experience

10+
Platform Users

10+
Clinical Sites

10+
Transforming Lives

Quantum is a next-generation eClinical platform designed to simplify and accelerate clinical research. Our integrated system combines clinical trial management software (CTMS), electronic data capture (EDC), eConsent software for clinical trials, and decentralized clinical trial platform capabilities into one unified solution.

Built for CROs, biotech, and pharmaceutical organizations, Quantum enables seamless clinical trial data collection software, real-time insights, and improved operational efficiency across the entire research lifecycle.

One Platform for All Your

Clinical Trial Requirements

Electronic Data Capture (EDC) Software for Clinical Trials

eTrialTrack’s Electronic Data Capture (EDC) software enables sponsors, CROs, and research sites to collect, manage, and validate…
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eConsent Software for Digital Clinical Trial Consent

eTrialTrack’s eConsent software enables sponsors, CROs, and research sites to digitize the informed consent process through secure,…
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Electronic Patient-Reported Outcomes (ePRO) Software

eTrialTrack’s ePRO software enables patients to report health outcomes directly through mobile and web applications, improving accuracy…
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eSource Software for Electronic Clinical Data Capture

eTrialTrack’s eSource software enables clinical sites to capture data directly at the source electronically. eSource replaces paper-based…
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eTMF Software for Clinical Trial Document Management

eTrialTrack’s eTMF software securely manages all clinical trial documents in a centralized digital repository. eTMF (Electronic Trial…
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RTSM Software for Clinical Trial Randomization & Supply

eTrialTrack’s RTSM software ensures precise patient randomization and efficient clinical supply chain management. RTSM (Randomization and Trial…
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About eTrialTrack

A Unified, Integrated e-Clinical Research Solutions

Built with decades of industry experience and a vision of creating one seamless solution to speed up the start and completion of clinical trials, reduce costs, and increase accuracy & efficiency — eTrialTrack ensures compliance and data security for a successful trial.

Clinical Data Collection Clinical IP Management Patient Engagement Data Analytics
  • Real-time data entry
  • Electronic CRF support
  • Source data verification
  • Automated medical coding
  • Remote data monitoring
  • Regulatory-ready formats
  • Multi-site data capture
  • Role-based data control
  • Inventory tracking system
  • Real-time IP visibility
  • Expiry date monitoring
  • Shipment status updates
  • Temperature excursion alerts
  • Site-wise IP allocation
  • Reconciliation automation
  • Regulatory label management
  • SMS/email reminders
  • eConsent form access
  • Real-time visit updates
  • Mobile-friendly interfaces
  • Telehealth visit support
  • Feedback collection tools
  • Educational content delivery
  • Multilingual communication
  • Dashboard-based insights
  • Adverse event tracking
  • Protocol deviation alerts
  • Query trend analysis
  • Real-time KPIs display
  • Custom report generation
  • Data export features
  • Statistical analysis tools
Designed for efficient clinical trial digitalization and optimization

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.


    Industries We Work With

    CRO

    Providing integrated solutions that enhance operational efficiency, collaboration, and visibility across clinical trial management processes and workflows.

    Life Sciences

    Empowering pharmaceutical and biotech organizations with advanced clinical technology to accelerate research, development, and market readiness globally.

    Hospital

    Supporting hospitals and medical research centres with secure, compliant, and streamlined clinical study management solutions for efficient operations.

    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.

    01

    Unified eClinical Platform

    Manage all trial activities through one integrated system.
    02

    Faster Study Startup

    Configure and deploy studies quickly with minimal implementation effort.
    03

    Regulatory Compliance

    Built to support FDA 21 CFR Part 11, ICH-GCP, audit trails, and role-based access controls.
    04

    Real-Time Reporting & Analytics

    Monitor enrollment, site performance, study progress, and clinical data through centralized dashboards.
    05

    Scalable for Any Trial Size

    Support early-phase studies, multi-site research, and global clinical programs.
    06

    24/7 Global Support

    Dedicated support team available across time zones.

    Advancing Global Compliance Assurance

    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 combines Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), eConsent, RTSM/IWRS, ePRO, Telehealth, and patient engagement tools into a single solution for managing clinical trials efficiently.

    What is a Clinical Trial Management System (CTMS)?

    A CTMS is software designed to help sponsors, CROs, and research sites manage study planning, site activities, patient enrollment, monitoring, budgets, and reporting throughout the clinical trial lifecycle. eTrialTrack includes a fully integrated CTMS module for streamlined trial management.

    How does Electronic Data Capture (EDC) improve clinical trials?

    EDC software replaces paper-based data collection with secure digital forms, enabling real-time data entry, automated validation checks, faster monitoring, and improved data quality while reducing operational costs and study timelines.

    Is eTrialTrack compliant with regulatory requirements?

    Yes. eTrialTrack is designed to support FDA 21 CFR Part 11 requirements, audit trails, electronic signatures, role-based access controls, and industry best practices to help organizations maintain compliance and data integrity.

    What is eConsent software and why is it important?

    eConsent software digitizes the informed consent process, allowing participants to review, understand, and sign consent forms electronically. It improves participant engagement, enhances compliance, and simplifies consent management for research teams.

    Can eTrialTrack support decentralized clinical trials?

    Yes. eTrialTrack includes decentralized clinical trial capabilities such as Telehealth, eConsent, ePRO, remote monitoring, and patient engagement tools, enabling participants to take part in studies from virtually anywhere.

    Who can use eTrialTrack?

    eTrialTrack is designed for pharmaceutical companies, biotechnology organizations, Contract Research Organizations (CROs), hospitals, research institutions, and clinical research sites looking to digitize and optimize their trial operations.

    Can eTrialTrack be customized for different study types?

    Absolutely. The platform is highly configurable and can be tailored to support different therapeutic areas, study designs, trial phases, workflows, and reporting requirements without extensive development effort.

    How secure is the data stored in eTrialTrack?

    eTrialTrack uses secure cloud infrastructure, encrypted data transmission, role-based permissions, audit trails, and regular security controls to protect sensitive clinical trial data and ensure data confidentiality.

    How quickly can eTrialTrack be implemented?

    Implementation timelines vary depending on study complexity and requirements. However, eTrialTrack is designed for rapid deployment, allowing organizations to launch studies quickly while maintaining compliance and operational efficiency.

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