Audience

Study-operations teams, clinical-trial sponsors and CROs searching for a solution to streamline site, enrollment, budget and milestone management across complex trial portfolios

About cubeCTMS

cubeCTMS is a comprehensive clinical-trial management system designed to provide end-to-end oversight of trials, from site and investigator tracking, enrollment management and visit scheduling through budget and contract workflows, milestone reporting and document control. It centralizes study operations and automates key processes so sponsors, CROs and study teams can monitor progress in real time, manage tasks across multiple studies, improve site communications and mitigate risk. With built-in dashboards, alerts and audit-ready logging, cubeCTMS supports regulatory compliance (including FDA 21 CFR Part 11 readiness) and enables stakeholders to manage trial timelines, resources and performance from one platform. The system integrates with other CRScube modules (such as EDC, eTMF, pharmacy/RTSM) to provide a unified ecosystem that reduces duplication, improves data flow and supports adaptive workflows during amendments or global roll-outs.

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Integrations

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Company Information

CRScube
Founded: 2010
South Korea
www.crscube.io/solution/cubectms

Videos and Screen Captures

cubeCTMS Screenshot 1
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Product Details

Platforms Supported
Cloud
Training
Documentation
Live Online
In Person
Videos
Support
Phone Support
Online

cubeCTMS Frequently Asked Questions

Q: What kinds of users and organization types does cubeCTMS work with?
Q: What languages does cubeCTMS support in their product?
Q: What kind of support options does cubeCTMS offer?
Q: What other applications or services does cubeCTMS integrate with?
Q: What type of training does cubeCTMS provide?

cubeCTMS Product Features

Clinical Trial Management

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