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
Explore the distinct advantages of nQuery, from sample size and power analysis to innovative adaptive trial design, and experience the ultimate trial design platform that accelerates clinical trials while reducing expenses and enhancing success rates. Learn why nQuery is the preferred option for researchers and biostatisticians globally, who are faced with the challenges of growing trial complexity, escalating costs, and evolving regulations. Effortlessly calculate sample sizes for FDA and EMA submissions with our quick, spreadsheet-style interface that requires no coding skills. We cater to both Frequentist and Fixed-term trials, providing straightforward reporting for all stakeholders involved in the trial process. Gain realistic forecasts of expected timelines and costs, ensuring your sample size aligns with both scientific and financial parameters. With the ability to fine-tune calculations using the multiple factors tool, nQuery offers over 1000 procedures for sample size and power calculations, enabling you to swiftly determine sample sizes across various scenarios, ultimately streamlining your clinical research efforts. Take advantage of nQuery's comprehensive features to navigate the complexities of modern clinical trials with confidence.
API Access
Has API
No
API Access
Has API
No
Integrations
R
No
RStudio
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
No
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
Yes
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
Statistical Solutions
Country
United States
Website
www.statsols.com
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
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