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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.

What is Certive?

Certive operates as a digital solution focused on product compliance and information management specifically designed for manufacturers, importers, distributors, and retailers. By integrating various components such as product and component profiles, bills of materials, supplier data, certificates, regulatory declarations, and documentation into a unified collaborative workspace, it streamlines operations. Teams have the capability to request essential documents from suppliers, track missing or expiring information, receive renewal notifications, evaluate compliance statuses, and maintain a history of audits. Certive supports compliance workflows for regulations including REACH, RoHS, CLP, CE marking, and SCIP, while also assisting in organizing information for Digital Product Passports. With the incorporation of AI-driven document validation, it helps identify any potential discrepancies that may warrant further review. Users can effectively prepare product documentation for audits as well as respond to customer inquiries, thereby managing product data across their supplier networks efficiently and ensuring regulatory compliance. This holistic method not only simplifies the compliance journey but also fosters improved collaboration and accountability among all stakeholders involved, creating a more transparent and efficient workflow. Ultimately, Certive positions itself as a vital tool in the modern regulatory landscape, empowering businesses to navigate complex compliance requirements with confidence.

Media

Media

No images available

Integrations Supported

Microsoft Excel
Microsoft Outlook

Integrations Supported

API Availability

Has API

API Availability

Has API

Pricing Information

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

Pricing Information

Pricing is scoped to product and component volumes, supplier network, regulatory requirements, and implementation and support needs. Proposals cover platform access and the agreed implementation, integrations, and support.

Supported Platforms

SaaS
Windows
On-Prem

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Online Training
On-Site Training

Company Facts

Organization Name

QT9 Software

Date Founded

2005

Company Location

United States

Company Website

qt9software.com/qms

Company Facts

Organization Name

Certive

Date Founded

2025

Company Location

Estonia

Company Website

www.certive.eu/

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

Categories and Features

Compliance

Not specified

Product Compliance

Not specified

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