Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
METS stands out as the premier solution for estimating projects and tracking materials, specifically designed as a web-based application for MEP contractors by industry experts. Its features foster collaboration and ensure accountability, making it the most thorough material management system tailored to MEP projects. With built-in systems for extensive validation and approval of various business processes, METS enhances the ability to "Delegate with Authorization," while still maintaining oversight and monitoring of all project activities. The application's analytical tools enable on-demand assessments, providing timely reports on project status and deviations, which helps teams make informed and accurate decisions swiftly. HVAC projects often face significant challenges such as managing the Scope of Work, reducing deviations, and appropriately delegating authority; METS effectively addresses these issues by providing precise estimation capabilities, strong change control management, and a framework for limited delegation of authority, making it an essential tool for ongoing project tracking and oversight. In essence, METS empowers teams to navigate the complexities of project management with confidence and accuracy.
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
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
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
SPD Enterprises
Founded
2009
Country
India
Website
metsystem.in
Vendor Details
Company Name
eDeviation
Website
www.protocoldeviation.com/eDeviation-software
Product Features
Construction Management
Accounting Integration
No
Budget Tracking/Job Costing
Yes
CRM
Yes
Change Orders
Yes
Commercial
Yes
Contract Management
Yes
Contractors
Yes
Equipment Tracking
Yes
Estimating
No
Incident Reporting
No
Mobile Access
Yes
Offline Access
Yes
RFI & Submittals
No
Residential
Yes
Subcontractor Management
Yes
Timesheets
No
MEP
3D Design
No
3D Spooling
No
Costing and Reporting
No
Design Feedback
No
Documentation Tools
No
Drafting Automation
No
HVAC Design
No
MEP Fabrication
No
Project Communication
No
Service Validation / Clash Detection
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