Get started with your free trial of QT9 QMS
QT9 QMS Free Trial Request
See QT9 QMS in action before your trial
Discover how QT9 QMS streamlines compliance and quality processes for regulated manufacturers. Schedule a personalized demo with our experts to see the platform configured for your workflows, and learn how your team can transition seamlessly into a full trial afterward.
FAQs: QT9 QMS Trial
The QT9 QMS trial gives you full access to 25+ integrated modules — including Document Control, CAPA, Audit Management, Training, Risk, and more. You can explore the same validated quality management software that organizations use to streamline compliance, automate processes, and drive continuous improvement.
Yes. You can configure forms, upload your own documents, and simulate real-world processes to see how QT9 QMS fits your operations. The trial runs in the same validated environment as the live system, so you can confidently evaluate workflows end-to-end.
QT9 QMS is available as both a cloud-based or on-premise solution, giving you flexibility to meet IT and compliance requirements. QT9 Software is ISO 27001 certified, ensuring industry-leading information security. Both options include full audit trails, role-based access, and FDA 21 CFR Part 11 compliance.
During your trial, you’ll have access to our embedded Help Center, user guides, training videos, and comprehensive documentation. Your sales rep will conduct both a pre-trial and post-trial walkthrough. Should you have any specific questions during the trial, you can reach out directly to your sales rep for assistance to help you get the most from your evaluation.
QT9 QMS is trusted by manufacturers in highly regulated industries, including medical device, pharmaceutical, life science, aerospace, and industrial manufacturing. The system is built to meet strict compliance standards while remaining flexible enough to support a wide range of manufacturing environments.
Yes. QT9 QMS automates compliance tasks such as document control, electronic approvals, audit tracking, and risk assessments to support ISO 9001, ISO 13485, FDA 21 CFR Part 11, and other quality management regulations.
Absolutely. You can invite multiple users to test workflows, assign tasks, and collaborate in real time. This lets your quality, engineering, and management teams experience how QT9 QMS improves visibility and communication across departments.
When you’re ready to move forward, QT9 Software converts your trial into a live system. All your data, configurations, and user permissions stay intact, allowing your organization to continue without downtime or data loss.
Yes — and we recommend it. Most companies begin with a personalized demo to see how QT9 QMS fits their quality and compliance processes. Our experts will walk your team through key modules and answer industry-specific questions. After the demo, you can start a full trial to explore the system hands-on with your own data.
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Call +1 630 892 5022
Or Call +1 866 913 5022
Email info@QT9software.com
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Wallace Ave
Point Cook VIC 3030
Call +61 03 8652 8677
Email sales@QT9softwaresolutions.com.au