Solutions

A unified clinical trial platform for EDC, eTMF, and CTMS — built for sponsors and CROs.

Primary platform solutions

EDC, eTMF, and CTMS

Electronic Data Capture
(EDC)

Centralize clinical trial data collection with a secure, configurable EDC designed for speed, accuracy, and regulatory compliance.

Electronic Trial Master File
(eTMF)

Maintain inspection-ready documentation with structured workflows, real-time completeness tracking, controlled access, and audit readiness.

Clinical Trial Management System (CTMS)

Available Q2 2026

Coordinate study operations, milestones, and oversight within a centralized CTMS designed to integrate seamlessly with EDC and eTMF workflows.

Platform Capabilies

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01. Optimized Workflows

Streamline your clinical trial process with a user-friendly platform designed for precision and efficiency at every stage.

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02. Compliance Made Simple

Effortlessly meet global regulatory standards with built-in validation and audit tools that support streamlined compliance.

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03. Flexible and Scalable

The platform is adaptable for every study, from pilot projects to large-scale global trials. Scale your processes as needed without compromising quality or efficiency.

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04. Centralized EDC System

Manage data collection and analysis in a single, secure EDC system, ensuring consistency and ease of access to critical trial information.

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05. ePRO Tools

Empower patients and researchers with ePRO tools designed to capture accurate clinical and patient-reported outcomes within the clinical trial platform.

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06. Digital Consent Solution

Simplify informed consent with a secure, regulatory-compliant eConsent system within the clinical trial platform, supporting comprehension and patient engagement.

Randomization and trial supply management tools

07. RTSM and Inventory Management Tools

Ensure reliable randomization and trial supply management with automated workflows and real-time notifications embedded within the platform.

eTMF - Electronic Trial Master Files

08. Electronic Trial Master File

Streamline clinical trial document management with our integrated electronic Trial Master File (eTMF) system.

Our eTMF provides centralized document control, automated filing, and real-time completeness tracking.

Explore Our Comprehensive EDC Solutions.

Optimized Workflows

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Explore Resource:
ICH E6(R2) Good Clinical Practice (GCP) Guidelines – International standards for electronic data capture (EDC), regulatory compliance, and clinical trial managemen