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.
Tele-Health
Participant Tracker
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.
eTrialTrack Features
Real-Time Data Entry & Access
Enhanced Data Accuracy & Compliance
Scalability & Flexibility
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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.
Empowering pharmaceutical and biotech organizations with advanced clinical technology to accelerate research, development, and market readiness globally.
Supporting hospitals and medical research centres with secure, compliant, and streamlined clinical study management solutions for efficient operations.
Why Choose eTrialTrack
eTrialTrack is a single-source, unified eClinical solution suite designed for efficient clinical trial digitalization and optimization, particularly tailored to the unique needs of small and midsize biopharma organizations.
21 CFR Part 11 Compliant
21 CFR Part 11 Compliant
Cloud Hosting
Cloud Hosting
Unified Platform
Unified Platform
Rapid Implementation
Rapid Implementation
24*7 Global support
24*7 Global support
Audit Trails
Audit Trails
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 a Clinical Trial Application (CTA)?
A CTA is a formal request submitted to regulatory authorities to obtain approval for conducting a clinical trial involving human participants.
Who needs to submit a CTA?
Sponsors such as pharmaceutical companies, biotech firms, medical device manufacturers or academic researchers must submit a CTA before starting a clinical trial.
What information is included in a CTA?
It typically includes study protocol, investigator details, patient information documents, investigational product details, safety data, and regulatory compliance statements.
Do different countries have different CTA requirements?
Yes, requirements vary by region. For example, the European Union requires a CTA under the Clinical Trial Regulation (CTR), while the US requires an Investigational New Drug (IND) submission.
Does the eTrialTrack support global CTA submissions (EU, US, Asia-Pacific, etc.)?
Yes, the platform is configurable to meet region-specific requirements such as EU-CTR CTIS submissions or US FDA IND equivalents.
Can one CTA cover multiple sites?
Yes, a single CTA can cover multiple trial sites within the same country, but ethics committee approvals are also required for each site.
Can the software handle country-specific document templates and regulatory forms?
The system comes preloaded with standard regulatory templates and allows customization for local authority formats.
Is there integration with other eClinical systems (EDC, eTMF, CTMS)?
Yes, seamless API-based integrations are available for real-time data exchange with trial management and documentation systems.
Does the solution provide audit trails for regulatory inspections?
Every action is time-stamped with user details and system-generated logs, ensuring full traceability.
Can the system generate submission-ready regulatory reports?
Yes, the platform auto-generates compliance-ready reports and authority-specific submission packages.