Average Ratings 0 Ratings

Total
ease
features
design
support

No User Reviews. Be the first to provide a review:

Write a Review

Average Ratings 0 Ratings

Total
ease
features
design
support

No User Reviews. Be the first to provide a review:

Write a Review

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 No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

No details available.

Integrations

No details available.

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 No 
Live Rep (24/7) No 
Online Support No 

Types of Training

Training Docs No 
Webinars No 
Live Training (Online) No 
In Person No 

Types of Training

Training Docs No 
Webinars No 
Live Training (Online) No 
In Person No 

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 No 
Document Filtering No 
Graphical Data Presentation No 
Language Detection No 
Predictive Modeling No 
Sentiment Analysis No 
Summarization No 
Tagging No 
Taxonomy Classification No 
Text Analysis No 
Topic Clustering 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 

Alternatives

Alternatives

Ember Reviews

Ember

MetiStream
ArcheMedX Ready Reviews

ArcheMedX Ready

ArcheMedX