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Average Ratings 0 Ratings

Total
ease
features
design
support

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Write a Review

Description

Verity enables Architecture, Engineering, and Construction (AEC) teams to produce precise quality evaluations on a large scale. It facilitates the automatic detection of discrepancies between your Autodesk Navisworks or Revit models and the as-built point cloud data, allowing for effective verification of the installation positioning or validation of model quality. By optimizing QA/QC processes, improving clash detection methodologies, and ensuring that the completed construction aligns with the planned design, you can minimize rework, avoid schedule delays, and mitigate overall project risks. The platform allows for straightforward comparisons between as-built point cloud data and your design or coordination models, enabling quick and accurate identification of errors in installation or modeling, whether at the level of individual components or larger scopes of work. This results in a more comprehensive and actionable analysis that is achieved significantly faster than traditional approaches. The system features customizable heat maps and color-coded reports that clearly illustrate deviations, bending, and deflection. Additionally, accurate measuring tools furnish quantitative data regarding how installed elements differ from your original models, providing deeper insights into project integrity. Ultimately, Verity not only enhances efficiency but also fosters confidence in the quality of the construction outcomes.

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

HTML Yes 
Navisworks Yes 
Revit Yes 

Integrations

HTML No 
Navisworks No 
Revit No 

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 No 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows Yes 
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 Yes 
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 Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person Yes 

Types of Training

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

Vendor Details

Company Name

ClearEdge3D

Country

United States

Website

www.clearedge3d.com/verity/

Vendor Details

Company Name

eDeviation

Website

www.protocoldeviation.com/eDeviation-software

Product Features

BIM

2D Drawing No 
3D Modeling No 
Change Management No 
Collaboration No 
Conflict Tracking No 
Design Modeling No 
Document Management No 
For Facility Management No 
Mobile Access No 
Scheduling 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 

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