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What is QUALITYWEB 360?

QUALITYWEB 360 provides 15 fundamental modules, such as Document Control, Internal Audits, Corrective Actions, and KPIs, aimed at ensuring adherence to ISO 9001 and related standards. This all-encompassing software allows for the management of all company processes within a single, centralized platform, delivering immediate insights that can boost productivity anytime and anywhere. Rely on our ISO 9001 software to manage the intricate tasks effectively, offering distinct advantages like mobile accessibility, strong data protection, and straightforward handling of certificates and acknowledgments. If you're on the lookout for an easy-to-use Quality Management System, QUALITYWEB 360 emerges as the perfect option, as its user-friendly interface guarantees seamless navigation for all users. Committed to enhancing operational efficiency, this software not only facilitates compliance but also enables your team to concentrate on what is most important—achieving high-quality outcomes. With its advanced features, QUALITYWEB 360 can transform the way your organization approaches quality management, making it a vital tool for sustained success.

What is QT9 QMS?

Streamline your quality processes with QT9's comprehensive cloud-based Quality Management System (QMS) Software Suite. Designed for ease of use, QT9 QMS features over 25 modules that offer unlimited scalability to meet your needs. Enhance your ISO and FDA compliance efforts with automated email alerts, task lists, and FDA 21 CFR Part 11 compliant electronic approvals. QT9 QMS empowers organizations in the Life Sciences, Biotechnology, Medical Device Manufacturing, and Pharmaceutical sectors to achieve digital transformation in their operations. Stay informed with real-time status updates and instantly visualize your quality metrics. The software includes essential features such as document control, revision management, corrective actions (CAPAs), and nonconformance tracking, among others. Additionally, it facilitates streamlined product releases with modules for Deviation Management, Engineering Change Orders, Failure Mode and Effects Analysis (FMEA), and Inspection Management. Transition to a paperless environment and automate your labor-intensive tasks effortlessly. QT9 QMS is ready for immediate use, allowing you to get started quickly. Experience it firsthand by signing up for a free product tour or beginning your free trial today at QT9qms.com. Embrace the future of quality management and elevate your organization's efficiency.

Media

Media

Integrations Supported

Integrations Supported

Microsoft Excel
Microsoft Outlook

API Availability

API Availability

Has API

Pricing Information

$50 per month

Pricing Information

$10,000/year
Includes all 25+ Modules. Unlimited Training and Support Available. Get a quote today.
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS
Windows
On-Prem

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Standard Support
Web-Based Support

Training Options

Documentation Hub

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

QUALITYWEB 360

Date Founded

2010

Company Location

Mexico

Company Website

www.qualityweb360.com

Company Facts

Organization Name

QT9 Software

Date Founded

2005

Company Location

United States

Company Website

qt9software.com/qms

Categories and Features

Compliance

Audit Management
Environmental Compliance
FDA Compliance
ISO Compliance
OSHA Compliance
Risk Management
Version Control

Customer Satisfaction

Analytics
Complaint Monitoring
Feedback Collection
Survey Management

Document Databases

Not specified

Document Management

Collaboration Tools
Compliance Tracking
Document Indexing
Electronic Signature
Version Control

Document Version Control

Access Controls/Permissions
Approval Process Control
Audit Trail
Revision History
Version Comparison

ISO Compliance

Not specified

Categories and Features

Calibration Management

Calibration Instructions
Calibration Schedules
Compliance Management
Device History
Due Date Tracking
Gage Management
Label Printing
Measurement Readings
Multi-Station Management
Out-of-Tolerance Notification
Statistical Data Reporting

CAPA

Audit Management
CAPA Planning
Change Management
Complaint Management
Incident Management
Nonconformance Tracking
Quality Control
Risk Management
Root Cause Analysis
Training Management

Compliance

Archiving & Retention
Audit Management
Compliance Tracking
Controls Testing
Environmental Compliance
FDA Compliance
ISO Compliance
Incident Management
OSHA Compliance
Risk Management
Surveys & Feedback
Version Control
Workflow / Process Automation

Document Control

Archiving & Retention
Automated Routing
Change Management
Compliance Management
Electronic Signature
Escalation Management
Periodic Review
Version Control

Document Version Control

Access Controls/Permissions
Approval Process Control
Archiving & Retention
Audit Trail
Commenting / Notes
Document Check-in / Check-out
For Engineering Documents
Revision History
Version Comparison
Version Rollback

FMEA

Not specified

Inspection

Appointment Management
Customer Database
Dispatch Management
Equipment Tracking
Photos In Reports
Print on Site
Report Templates
Subcontractor Management

ISO Compliance

Not specified

Life Sciences

Not specified

Product Compliance

Not specified

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management

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