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What is cubeCDMS?
cubeCDMS serves as an all-encompassing electronic data capture platform meticulously designed for the efficient handling of clinical trial operations, significantly improving the data collection and monitoring process. This sophisticated system integrates complete data management workflows that include automatic identification of protocol violations, query batch management, and risk-based monitoring, all of which work together to enhance data integrity and operational efficiency. Featuring a user-friendly, no-code interface, research teams can easily develop electronic case report forms (eCRFs) from a library of over 55 pre-built forms and edit checks, leading to rapid database configurations and reduced start-up durations. Additionally, cubeCDMS is designed for user convenience, allowing for single data entry that is seamlessly shared across various integrated CRScube modules, which effectively reduces redundancy and simplifies the reconciliation process. Beyond this, it presents numerous benefits such as AI-driven medical coding support, intuitive drag-and-drop tools for form creation, multilingual support, and thorough audit trails along with change history tracking, all ensuring transparency and dependability throughout the trial lifecycle. Ultimately, this cutting-edge solution enables clinical researchers to concentrate more on their investigative efforts while refining their data management strategies, thus enhancing the overall efficacy of clinical trials. Additionally, its integration capabilities allow for greater collaboration among teams, further streamlining the research process.
What is SimpleTrials?
SimpleTrials is a subscription-based, on-demand Clinical Trial Management System (CTMS) specifically designed for sponsors, Contract Research Organizations (CROs), and research facilities. It offers a comprehensive suite of tools that streamline the planning, management, and oversight of clinical study portfolios, including features for site initiation, subject monitoring, and document management via an integrated electronic Trial Master File (eTMF). Users can take advantage of real-time analytics for their studies, detailed calendars, customizable fields and trackers, on-demand reporting, planning milestones, and the management of site contracts and payments, along with electronic documentation of visits. The platform is constructed to adhere to 21 CFR Part 11 compliance standards, providing a secure and validated environment for the handling of clinical trial data. Additionally, users can customize their tracking views, seamlessly connect with various Electronic Data Capture (EDC) systems, and utilize pre-built templates for consistent document management. By fostering enhanced collaboration among all stakeholders, the system supports more effective communication throughout the entirety of the trial process, ultimately leading to improved outcomes and efficiency in clinical research.
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
$849 per month
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/cubecdms
Company Facts
Organization Name
SimpleTrials
Date Founded
2008
Company Location
United States
Company Website
www.simpletrials.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
Electronic Data Capture
Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management
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