Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
CIMS Global delivers advanced data science platforms and eClinical solutions that are set to transform the landscape of clinical trials by enhancing the quality, efficiency, and speed of processes like data acquisition, processing, analysis, monitoring, and regulatory submissions. Their offerings feature groundbreaking tools such as CRE, DDM, DMC-HUB, and eBinder, as well as a comprehensive eClinical Suite that facilitates data collection, analytics, and clinical functions throughout all phases of a trial. CRE serves as a multi-tenant, validated Statistical Computing Environment specifically designed for compliant analysis of clinical data, leveraging R, RShiny, and the RStudio IDE within a secure framework ready for audits that aligns with 21 CFR Part 11 and GxP regulations. DDM stands out as a patented Dynamic Data Monitoring platform that visualizes cumulative treatment effects on a trial radar screen while also forecasting the likelihood of a trial’s success or failure. Additionally, the integration of these innovative solutions positions CIMS Global at the forefront of clinical trial technology, ensuring that researchers can achieve optimal outcomes in their studies.
Description
Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.
API Access
Has API
No
API Access
Has API
No
Pricing Details
No price information available.
Free Trial
Yes
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
No
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
CIMS Global
Founded
2004
Country
United States
Website
cims-global.com
Vendor Details
Company Name
Merative
Founded
2022
Country
United States
Website
www.merative.com/clinical-development
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No
Data Science
Access Control
No
Advanced Modeling
No
Audit Logs
No
Data Discovery
No
Data Ingestion
No
Data Preparation
No
Data Visualization
No
Model Deployment
No
Reports
No
Electronic Data Capture
Audit Trail
No
CRF Tracking
No
Data Entry
No
Data Verification
No
Distributed Capture
No
Document Imaging
No
Document Indexing
No
Forms Management
No
Remote Capture
No
Study Management
No
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Yes
Document Management
Yes
Electronic Data Capture
Yes
Enrollment Management
Yes
HIPAA Compliant
Yes
Monitoring
Yes
Patient Database
No
Recruiting Management
Yes
Scheduling
Yes
Study Planning
Yes
Electronic Data Capture
Audit Trail
Yes
CRF Tracking
Yes
Data Entry
Yes
Data Verification
Yes
Distributed Capture
Yes
Document Imaging
Yes
Document Indexing
Yes
Forms Management
Yes
Remote Capture
Yes
Study Management
Yes