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What is CORE (Clinical On-demand Research)?

CORE (Clinical On-demand Research) offers an extensive range of specialized services that include the design, development, and management of electronic forms used in clinical trials across the UK and globally. Beyond creating the essential forms, CORE also manages randomization processes, data oversight, and provides vital study statistics, ensuring that researchers have the key information they need. This organization plays a critical role in gathering significant data for both academic and commercial research sectors. Notably, CORE has formed a successful partnership with FormsVision, which originated from an FP7 EU funding initiative, and has integrated the ALEA eCRF (electronic Case Report Form) to improve trial execution in the UK and New Zealand. The dedicated team at CORE is prepared to deliver a wide range of services, which encompass database development for CRFs, management of randomizations, coordination of drug supplies, and ePRO (ALEA) solutions. They also provide data hosting services for various file types and offer expert assistance with funding applications, statistical analysis, and protocol development. By delivering this comprehensive array of services, CORE solidifies its role as an essential collaborator in the progression of clinical research initiatives. Their commitment to enhancing research methodology and data integrity further underscores the importance of their contributions to the field.

What is CIMS Global?

CIMS Global offers cutting-edge data science platforms and eClinical solutions aimed at revolutionizing the clinical trial landscape by improving the quality, efficiency, and speed of key processes such as data collection, analysis, monitoring, and regulatory submissions. Their suite of innovative tools includes CRE, DDM, DMC-HUB, and eBinder, along with a complete eClinical Suite designed to support data gathering, analytics, and clinical operations throughout every stage of a trial. Specifically, CRE functions as a multi-tenant, validated Statistical Computing Environment tailored for compliant clinical data analysis, utilizing R, RShiny, and the RStudio IDE within a secure audit-ready framework that complies with 21 CFR Part 11 and GxP regulations. DDM emerges as a patented Dynamic Data Monitoring platform that provides visual insights into cumulative treatment effects through a trial radar screen while also predicting the likelihood of trial success or failure. Moreover, the seamless integration of these advanced solutions not only reinforces CIMS Global's leading position in clinical trial technology but also empowers researchers to attain the best possible outcomes in their studies. This commitment to innovation ensures that every aspect of clinical trial management is streamlined and data-driven.

Media

Media

Integrations Supported

R
RStudio

Integrations Supported

R
RStudio

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

CIRU, University of Southampton

Date Founded

2000

Company Location

United Kingdom

Company Website

www.the-ciru.com/core

Company Facts

Organization Name

CIMS Global

Date Founded

2004

Company Location

United States

Company Website

cims-global.com

Categories and Features

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

Data Science

Access Control
Advanced Modeling
Audit Logs
Data Discovery
Data Ingestion
Data Preparation
Data Visualization
Model Deployment
Reports

Electronic Data Capture

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

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