cubeCDMS

cubeCDMS

CRScube
+
+

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About

Create, in a few hours, an eCRF that is as easy to use as a paper one, and avoid the biggest headaches in data collection in Pre-authorisation and Post-authorisation studies of your medical device. Incorporate an EDC that is highly flexible when creating the eCRF, this will allow you to meet the needs of any kind of study. Save tons of time in the management and monitoring of the study with the management and monitoring tools included in the EDC. Use a validated system with all the security guarantees that give trust to the sponsor and allow the collection of quality data. Don’t wait until the analysis phase to discover mistakes in the data or you will end up chasing down investigators to correct them. Prevent the process of creation of an eCRF from being long and complex.

About

cubeCDMS is an electronic data capture solution designed for clinical trial operations that streamlines the end-to-end data collection and management workflow. The system supports full data-management workflows including automatic protocol-violation detection, batch query management and native risk-based monitoring to help improve data quality and operational efficiency. The intuitive, no-code user interface enables study teams to build eCRFs (electronic case report forms) from a library of more than 55 ready-to-use forms and edit checks, quickly set up the database, and reduce start-up time. Designed for usability, cubeCDMS allows data entry once and flows data seamlessly across other integrated CRScube modules, reducing redundancy and reconciliation. Additional benefits include AI-powered medical-coding support, drag-and-drop form builders, multi-language support, and robust audit trails and change-history tracking.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Clinics searching for a CRF electronic service to collect and manage data for clinical trials and multi-site patient registries

Audience

Clinical data managers, CROs and sponsors seeking a solution to accelerate clinical data capture, ensure compliance and boost data integrity

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

$500/month
Price only based on number of participants and required add-ons. There is no limit to the number of sites or users.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 4.7 / 5
ease 4.7 / 5
features 4.3 / 5
design 4.3 / 5
support 4.8 / 5

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Pros & Cons from Real Users

Pros

  • The platform fit all our needs, the team was very flexible and very attentive to all our comments and questions during and after the process.
  • It is really intuitive and let adapt our needs. The menu is very complete which let know the state of each patient
  • The attention and support of your team for any problem or unforeseen event. How intuitive the platform is for research teams.
  • User-Friendly Interface: The system is easy to navigate, requiring minimal training for site personnel and monitors. This leads to quicker adoption and fewer user errors. Balancing Functionality and Cost ShareCRF: Enhancing Clinical Trial Efficiency with an Intuitive EDC System
  • Technical assistance and customer service are supreme. User-friendly and very easy to configure for all parties involved in the study.

Cons

  • We have no complaints, we did encounter some issues but every time the team fixed it pretty quickly.
  • Anything, and we trust in their capacity to keep improving
  • It is difficult for me to point this out but it may be the lack of customisation when downloading PDFs.
  • Reporting features may be less robust compared to other premium EDC systems, potentially limiting the depth of data insights available directly within the platform.
  • For some of the settings the possibilities are limited and therefore the analysis of the data retrieved is not flexible enough.

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

ShareCRF
www.sharecrf.com

Company Information

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

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cubeCDMS

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Categories

Categories

Clinical Trial Management Features

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 Features

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Integrations

IBM SPSS Statistics
Microsoft Excel
SAS Analytics Pro
cubeCTMS
cubeSAFETY

Integrations

IBM SPSS Statistics
Microsoft Excel
SAS Analytics Pro
cubeCTMS
cubeSAFETY
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