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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 ImproWise?

ImproWise is a fully online platform that ensures both security and compliance with HIPAA regulations, specifically crafted for all-encompassing Clinical Trial Management Systems (CTMS) and Clinical Data Management Systems (CDMS). This cutting-edge solution offers unparalleled adaptability, swift performance, and strong security by merging features such as CTMS, CDMS, Electronic Data Capture (EDC), Clinical Trial Budget Management (CTBM), Clinical Trial Project Management (CTPM), electronic Trial Master File (eTMF), electronic Patient Reported Outcomes (ePRO), and Role-Based Access Control Systems (RBACS). Designed to meet the diverse needs of all stakeholders in clinical trials, ImproWise promotes seamless collaboration among sponsors, investigators, data managers, data entry personnel, site staff, and regulatory affairs specialists, thereby improving efficiency across the entire trial process. In addition, the platform's intuitive interface is user-friendly, making it easy for individuals with varying levels of technical expertise to engage effectively in the trials. This accessibility empowers all contributors to focus on their roles without being hindered by technological barriers. Ultimately, ImproWise stands out as a vital tool in advancing clinical research and achieving successful trial outcomes.

Media

Media

No images available

Integrations Supported

cubeCDMS
cubeSAFETY

Integrations Supported

cubeCDMS
cubeSAFETY

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
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

Core Clinical Services

Company Location

India

Company Website

improwisetrials.com

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

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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