Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
CluePoints offers a cloud-based platform that utilizes AI for risk-based quality management and oversight of clinical data, employing sophisticated techniques like machine learning and deep learning to enhance the reliability, precision, and safety of data and processes in clinical trials. This platform stands out with its capability for real-time anomaly detection and centralized statistical monitoring, effectively spotting outliers and data risks that conventional methods may overlook, thereby empowering teams to proactively address risks and expedite the resolution of issues while adhering to FDA, EMA, and ICH standards. Additionally, CluePoints features tailored solutions including Risk-Based Quality Management (RBQM) for timely risk identification, Medical & Safety Review (MSR) for efficient review and query management, Intelligent Medical Coding for automated clinical coding suggestions, and Intelligent Query Detection (IQD) to facilitate the detection of discrepancies, along with tools like the Site Profile & Oversight Tool (SPOT) designed for dynamic site monitoring to ensure optimal oversight throughout the trial process. These advanced features collectively contribute to improving the overall efficiency and effectiveness of clinical trials.
Description
The Medidata Clinical Cloud represents our innovative platform designed to revolutionize the clinical trial journey for patients, sponsors, CROs, and research institutions. As the sole comprehensive technology solution focused exclusively on clinical research, the Medidata Clinical Cloud addresses the entire research spectrum from inception to completion. Our platform enables organizations in the life sciences and medical device sectors to reduce development expenses, manage risks effectively, and expedite the introduction of treatments and devices to the marketplace. Whatever selection you make for your clinical trial initiatives, you will benefit from the capabilities of the Medidata Clinical Cloud. At Medidata, we are at the forefront of the digital evolution in clinical research. With the power of artificial intelligence, machine learning, and sophisticated analytics, our platform connects researchers, study coordinators, investigators, and patients, thereby hastening the research process. Additionally, it provides a regulatory-compliant, patient-friendly electronic informed consent solution for clinical trials, ensuring a smoother experience for all parties involved. This integration of advanced technology not only streamlines operations but also enhances the overall quality of clinical research.
API Access
Has API
No
API Access
Has API
No
Integrations
BioGRID
No
ClinVigilant
No
Datavant
No
Greenlight Guru Clinical
No
Rave CTMS
No
Rave EDC
No
Integrations
BioGRID
Yes
ClinVigilant
Yes
Datavant
Yes
Greenlight Guru Clinical
Yes
Rave CTMS
Yes
Rave EDC
Yes
Pricing Details
No price information available.
Free Trial
No
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
No
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)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
No
In Person
Yes
Vendor Details
Company Name
CluePoints
Founded
2012
Country
United States
Website
cluepoints.com/what-we-do/
Vendor Details
Company Name
Dassault Systèmes
Founded
1981
Country
France
Website
www.medidata.com/en/clinical-trial-products/unified-platform
Product Features
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