Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
Advanced clinical data analytics is essential for expediting and minimizing risks associated with regulatory approvals, thanks to our innovative automated analytics and validation platform. Unlike any other clinical data analytics software, our solution enhances data integrity and reduces the risks tied to submissions. By automating manual quality processes, you can avoid the hassle of QC reruns, eliminate instances of data duplication and inconsistencies, and maintain robust data traceability, all while ensuring a transparent quality assurance process. This leads to a faster time to market, allowing businesses to generate revenue sooner and reduce validation times effectively. Moreover, this efficiency frees up valuable resources and cuts costs, thereby accelerating the journey to regulatory approval. The demand for precise clinical data validation and top-tier data output is increasingly critical in today’s fast-paced environment. Verify is dedicated to managing and analyzing clinical data to minimize risk and hasten the approval process for new drugs and vaccines, ensuring that quality, speed, and success are at the forefront of your clinical trials. Ultimately, our platform empowers organizations to respond swiftly to market needs while maintaining high standards of compliance.
Description
eDeviation provides comprehensive tools for assessing and managing Protocol Deviations. It streamlines processes from software design and validation to gathering necessary documentation and exporting information for the Trial Master File (TMF), thereby alleviating the burden on clinical teams who may face risks from improperly assessed or overlooked protocol deviations, whether they occur once or multiple times. As a component of Ethical's eClinical Software Platforms, eDeviation® enhances the efficiency and accuracy of clinical trial management. Whether evaluations are conducted by a dedicated independent committee or by your own research team, our software can be tailored to meet your specific requirements. The integration of forms, workflows, and export functions ensures adherence to GxP standards and fosters effective study management. Additionally, this platform allows study teams, investigators’ sites, and committee members to collaborate online in real-time, facilitating quicker decision-making, reaching consensus, and ensuring the prompt handling of protocol deviation assessments and management. Ultimately, eDeviation® enhances the overall integrity and efficiency of clinical trial processes, contributing to better outcomes in research.
API Access
Has API
API Access
Has API
Integrations
No details available.
Integrations
No details available.
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Beaconcure
Founded
2016
Country
Israel
Website
beaconcure.com
Vendor Details
Company Name
eDeviation
Website
www.protocoldeviation.com/eDeviation-software
Product Features
Text Mining
Boolean Queries
Document Filtering
Graphical Data Presentation
Language Detection
Predictive Modeling
Sentiment Analysis
Summarization
Tagging
Taxonomy Classification
Text Analysis
Topic Clustering
Product 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