Clinical Trial Management System

A robust and scalable platform to streamline trial planning, data capture, monitoring, and reporting, crafted for CROs, hospitals, and pharma innovators.

< TrialCore >

From Protocol to Data, Streamlined Trials That Scale

Our Clinical Trial Management System is built to simplify and digitize the clinical research lifecycle. Whether you’re managing a single-site study or a global, multi-phase trial, our platform provides secure data access, workflow automation, real-time monitoring, and comprehensive reporting. Designed with the needs of modern CROs and pharma R&D teams in mind, it integrates seamlessly with EDC platforms and regulatory systems. From site tracking and participant scheduling to budget management and compliance documentation, this solution aligns with evolving research demands. We are your technology partner for dependable clinical software solutions, designed to advance accuracy, speed, and efficiency in trial operations.

< MedUse >

Clinical-Grade Adaptability. Real-World Results.

Whether for oncology, vaccines, or behavioral studies, our platform is adaptable to any research domain or regulatory region.

Phase I Trials

Track dosage escalation, safety monitoring, and subject enrollment with high accuracy.

Multi-Site Study Management

Monitor multiple trial locations with centralized dashboards and role-based access.

Oncology Research

Capture longitudinal data and biomarkers using integrated clinical data management software.

Device Trials

Document approvals, performance logs, and adverse events for medical device testing.

Remote Trials & Telehealth Studies

Integrate eConsent, remote monitoring, and virtual site visits for decentralized studies.

Regulatory Compliance Modules

Built-in documentation and audit logs ensure FDA, EMA, and ICH-GCP readiness.

< TrialROI >

More Insight, Less Overhead

Our pricing structures allow CROs, research labs, and sponsors to scale operations without scaling costs.

SaaS Licensing

Monthly/annual subscriptions for unlimited trials and multi-user teams.

Per-Site Activation Fee

Charge based on the number of clinical research locations onboarded.

Role-Based User Plans

Pay only for advanced roles, monitor, coordinator, investigator, or admin.

Per-Study Model

Ideal for smaller organizations managing studies one at a time.

EDC Integration Premium

Add-on pricing for integrating EDC in clinical research workflows.

Custom Enterprise License

One-time pricing for large pharma with long-term usage.

SaaS Licensing

Monthly/annual subscriptions for unlimited trials and multi-user teams.

Per-Site Activation Fee

Charge based on the number of clinical research locations onboarded.

Role-Based User Plans

Pay only for advanced roles, monitor, coordinator, investigator, or admin.

Per-Study Model

Ideal for smaller organizations managing studies one at a time.

EDC Integration Premium

Add-on pricing for integrating EDC in clinical research workflows.

Custom Enterprise License

One-time pricing for large pharma with long-term usage.

< DataVitals >

Every Click Is Clinical Precision

From scheduling and compliance to real-time data review, our platform delivers features that empower every role in the research lifecycle.

Protocol Templates

Real-Time Data Validation

Role-Based Access Control

Custom Form Builders

EDC Platform Integrations

Regulatory Document Management

< Tech Stack >

Built to Advance Research, Backed by Scalable Tech

Our clinical research platform is built on a Node.js/Express backend with MongoDB for scalable data storage and PostgreSQL for transactional integrity. Frontend dashboards are powered by Angular and React. We use AWS for cloud hosting and disaster recovery, with enhanced data security and audit controls. Our clinical trial data management software modules integrate with third-party EDCs and analytics engines using secure REST APIs. With HIPAA and GDPR-compliant data handling, our stack is engineered for global research excellence.