QT9 QMS Overview
Take a quick interactive tour of QT9 QMS and see how teams can centralize quality processes, improve visibility, and manage compliance in one connected system.
Most Manufacturers research QMS and ERP solutions for 6-18 months before talking to a vendor. Take the 3-minute readiness check to find exactly where your data is breaking down before any sales conversation.
Click through live walkthroughs of QT9 QMS and QT9 ERP. See exactly how the platform works before talking to anyone on our team.
Start with the free overview, then unlock focused walkthroughs for key quality workflows.
Take a quick interactive tour of QT9 QMS and see how teams can centralize quality processes, improve visibility, and manage compliance in one connected system.
See how QT9 QMS helps teams manage document approvals, revisions, access, and version control with a streamlined digital workflow.
Unlock TourExplore how QT9 QMS simplifies calibration scheduling, equipment tracking, due dates, and compliance documentation.
Unlock TourWalk through how teams can track ISO-related actions, assign responsibilities, monitor progress, and support continuous improvement.
Unlock TourAnswer a few quick questions to estimate the potential annual cost of scrap, rework, holds, supplier issues, and investigation delays.
Thousands of users rely on QT9’s top-rated software to simplify compliance, reduce manual work and improve operational efficiency. QT9 is recognized on G2 for ease of use, support and rapid ROI.
For regulated manufacturers moving away from spreadsheets, standalone tools and disconnected data. Start with one product — add the other when your team is ready.
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QT9 QMS manages quality and compliance workflows like document control, CAPA, audits, training management, calibration and supplier quality. QT9 ERP manages operations including inventory, purchasing, production scheduling, traceability, maintenance and accounting. Many manufacturers start with one system and later connect both platforms for a fully integrated quality and operations environment.
Yes. QT9 is designed for regulated industries including medical device, pharmaceutical, aerospace, automotive, food & beverage and general manufacturing companies that need compliance visibility and operational control. QT9 supports standards such as ISO 9001, ISO 13485, AS9100, FDA 21 CFR Part 11, IATF 16949 and FSMA.
Absolutely. This page includes interactive product tours so you can explore QT9 QMS and QT9 ERP at your own pace without speaking to sales first. You can click through real workflows, modules and dashboards to better understand how the platform works before requesting a personalized demo.
Most QT9 implementations are significantly faster than traditional enterprise systems. QT9 QMS deployments can take as little as 30 days, depending on company size, workflows and validation requirements. QT9 ERP timelines vary based on operational complexity and integrations.
Yes. Many manufacturers use QT9 to eliminate spreadsheets, manual audit preparation, disconnected quality records and siloed operational data. QT9 centralizes quality management and manufacturing workflows into one connected cloud platform with real-time visibility and traceability.
QT9 automates workflows such as document approvals, CAPA routing, audit findings, calibration scheduling, maintenance tracking, supplier corrective actions, employee training assignments, inventory holds, production traceability and management reporting. Automated workflows help reduce manual work while improving compliance consistency across teams.
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