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.
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.
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.
Clinical Trial Requirements
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
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.
- 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
eTrialTrack Features
Real-Time Data Entry & Access
Enhanced Data Accuracy & Compliance
Streamlined Study Design
Scalability & Flexibility
Improved Monitoring & oversight
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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.
Unified eClinical Platform
Faster Study Startup
Regulatory Compliance
Real-Time Reporting & Analytics
Scalable for Any Trial Size
24/7 Global Support
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.