eTrialTrack
e-Clinical Research Solutions
Speeding up the start and completion of clinical trials, reducing costs, and increasing accuracy & efficiency…built with decades of industry experience and one seamless solution.
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.
A Unified, Integrated, Intelligent Platform that Provides tools to meet all business requirements for any EDC Clinical Study
Tele-Health
Participant Tracker
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.
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
Our EDC solutions are purpose-build for clinical trials. They enable real-time data entry, automatic validation checks and seamless data access across trial sites. This not only enhance data quality and integrity but also accelerates trial timelines and decision-making.
Our EDC solutions are purpose-build for clinical trials. They enable real-time data entry, automatic validation checks and seamless data access across trial sites. This not only enhance data quality and integrity but also accelerates trial timelines and decision-making.
📅 Book a Demo or 📥 Download our brochure to learn more about how we help clinical teams achieve faster, safer, and more patient-friendly clinical Trials.
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.
