QT9 QMS is an all-in-one quality management software suite that helps organizations centralize and automate their quality processes such as document control, audits, training, risk management and CAPA. It supports many industries from medical devices and pharmaceuticals to manufacturing and aerospace and is scalable for small businesses and enterprises.

Is the demo free and can I try QT9 QMS with real data?

Yes. After the demo you can start a free trial that provides full access to 25+ integrated modules. You may upload real company documents and configurations to test actual workflows. No credit card is required to begin the trial.

What types of quality-management modules does QT9 QMS include?

QT9 QMS includes 25+ modules such as Document Control, Audit Management, CAPA, Risk Management, Nonconforming Products, Quality Event Management, Supplier and Customer Portals, Training Management, Equipment and Calibration Management, Change Control, Inspections and Project Management.

Can QT9 QMS help support compliance with ISO and FDA standards?

QT9 QMS supports compliance-related functions for standards such as ISO 9001, ISO 13485, FDA 21 CFR Part 11, AS9100, IATF 16949 and others by automating document control, audit trails, e-signatures, change control, risk assessment and corrective actions.

Does QT9 QMS offer training and support for new users?

Yes. QT9 provides unlimited training and support through online documentation, a knowledge base, webinars and a support system which helps organizations onboard staff and maintain compliance without extra licensing fees.

Request a QMS Software Demo | See the QT9 Quality Management System

Q: What does the QT9 QMS demo offer?

The demo lets prospective users request a personalized walkthrough of QT9 QMS in action. You can see how core modules including document control, audit management, CAPA, training, risk and compliance workflows perform in a realistic setup to understand how the software could integrate into your operations.

Q: Which industries is QT9 QMS suitable for?

QT9 QMS is suitable for regulated and industrial sectors including medical devices, pharmaceuticals, life sciences, aerospace, automotive, chemicals, cosmetics, food and beverages, manufacturing, plastics and other industries needing structured quality and compliance processes.

Q: What are some benefits of using QT9 QMS over traditional quality-management tools like spreadsheets and email chains?

By consolidating all quality processes into one system, QT9 QMS reduces manual errors, eliminates paperwork, improves visibility of quality and compliance data, accelerates workflows, enhances collaboration across departments and strengthens consistency and efficiency.

FAQ: QT9 QMS Demo

The demo page lets prospective users request a personalized walkthrough of QT9 QMS in action. During the demo you’ll see how core modules perform — including document control, audit management, CAPA, training, risk and compliance workflows — giving you a realistic view of how the software can fit into your operations.

Yes. After the demo, you can start a free trial that gives full access to 25+ integrated modules. You can upload your company’s own documents and configuration to test how the system handles real-world workflows. No credit card is required to begin the trial.

QT9 QMS includes 25+ modules such as Document Control, Audit Management, CAPA, Risk Management, Nonconforming Products, Quality Event Management, Supplier & Customer Portals, Training Management, Equipment & Calibration Management, Change Control, Inspections, Project Management and more.

QT9 QMS is suitable for regulated and industrial sectors, including medical devices, pharmaceuticals, life sciences, aerospace, automotive, chemicals, cosmetics, food & beverages, manufacturing, plastics and more.

Yes. QT9 QMS supports compliance-related functions for standards such as ISO 9001, ISO 13485, FDA 21 CFR Part 11 (and related FDA QSR regulations), AS9100, IATF 16949 and others — by automating document control, audit trails, e-signatures, change control, risk assessment and corrective actions.

By consolidating all quality processes in one system, QT9 QMS reduces manual errors, eliminates paperwork, improves visibility of quality and compliance data, accelerates workflows, enhances collaboration across departments and supports consistency — all of which lead to better efficiency, faster time to market and improved compliance.

Yes. QT9 includes unlimited training and support resources through online documentation, knowledge-base, webinars and a designated support system — helping organizations onboard staff and maintain compliance without extra licensing costs.