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What is cubeCTMS?

cubeCTMS serves as a comprehensive clinical trial management platform that ensures thorough supervision of trials, which includes monitoring study sites and investigators, handling participant enrollment and visit schedules, and managing budgets and contract workflows, along with milestone reporting and document oversight. By consolidating study operations and automating key processes, it enables sponsors, CROs, and research teams to track progress in real time, coordinate activities across multiple studies, improve communication with study sites, and mitigate risks. The platform features integrated dashboards, alerts, and audit-ready documentation to maintain compliance with regulatory requirements, including readiness for FDA 21 CFR Part 11, thus empowering stakeholders to manage trial schedules, resources, and overall performance from a unified interface. Furthermore, cubeCTMS effortlessly integrates with other modules of CRScube, such as EDC, eTMF, and pharmacy/RTSM, forming a harmonious ecosystem that reduces redundancy, enhances data flow, and accommodates flexible workflows during amendments or extensive implementations. This integration not only streamlines various processes but also significantly boosts the overall effectiveness of clinical trials, ultimately proving to be an essential asset for research teams dedicated to advancing medical knowledge. With its user-friendly design and robust features, cubeCTMS sets a new standard in clinical trial management solutions.

What is BizNet?

Accelerate clinical innovation with an AI-enabled Clinical Research Platform that unifies Early Phase CTMS, Late Phase CTMS, and Bioanalytical LIMS into a single, intelligent ecosystem. Purpose-built for pharmaceutical, biotechnology, and CRO organizations, the platform streamlines the complete clinical development lifecycle, from protocol planning, volunteer and patient management, site operations, study execution, and sample lifecycle management to bioanalytical testing, data review, and regulatory reporting. AI-powered capabilities such as intelligent workflow automation, predictive analytics, anomaly detection, smart data validation, and real-time decision support help research teams identify risks early, optimize resources, reduce manual effort, and make faster, data-driven decisions. A key differentiator is its unified CTMS-LIMS architecture, eliminating data silos while ensuring seamless data flow, end-to-end traceability, and operational transparency across clinical and laboratory functions. Configurable workflows, role-based dashboards, automated alerts, and enterprise integrations with EDC, eTMF, ERP, and laboratory instruments enhance collaboration and study oversight. Built on a scalable, GxP-compliant framework supporting GLP, GCP, and 21 CFR Part 11, the platform delivers audit-ready documentation, electronic records, secure access controls, and complete data integrity. By combining AI-driven intelligence with compliance, interoperability, and operational excellence, it empowers sponsors and CROs to accelerate trials, improve study quality, and bring therapies to market faster.

Media

Media

Integrations Supported

cubeCDMS
cubeSAFETY

Integrations Supported

API Availability

API Availability

Pricing Information

Pricing not provided

Pricing Information

$79
Contact Sarjen Systems Pvt Ltd.

Supported Platforms

SaaS

Supported Platforms

SaaS
Windows
On-Prem

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

CRScube

Date Founded

2010

Company Location

South Korea

Company Website

www.crscube.io/solution/cubectms

Company Facts

Organization Name

Sarjen Systems Pvt Ltd

Date Founded

1998

Company Location

India

Company Website

biznet.sarjen.com

Categories and Features

Categories and Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

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