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ISO 17025 quality management system for the competence of testing and calibration laboratories. Easily meet FDA regulations accurately and efficiently with the QT9™ QMS.
Keep track of laboratory compliance items and synchronize documentation with anyone, anywhere.
QT9 QMS reduces staff time by eliminating manual processes.
QT9 QMS collects & prioritizes all your ISO & ISO 17025 compliance.
QT9 QMS lets you upload, publish & distribute documents.
QT9 QMS helps you anticipate & address changes & problems.
QT9's ISO 17025 quality management system is your all-in-one ISO 17025 software solution.
QT9™ QMS Document Control Module
QT9™ QMS Management Review Module
QT9™ QMS Employee Training Module
QT9™ QMS Preventive Action Module
QT9™ QMS Risk Assessments Module
QT9™ QMS Engineering Change Request Module
QT9™ QMS Supplier Evaluation Module
QT9™ QMS Inspection Module
QT9™ QMS Calibration Module
QT9™ QMS Customer Feedback Module
QT9™ QMS Audit Management Module
QT9™ QMS Nonconforming Product Module
QT9™ QMS Corrective Actions Module
QT9's easy-to-use ISO 17025 quality management system makes laboratory traceability and transparency simple.
Quickly see the status of ISO 17025 items with real-time reports from the QT9 dashboard. You can even personalize the view specific to your needs.
Make approvals electronically with electronic signature capturing built-in. QT9's ISO 17025 quality management system is 21 CFR Part 11 compliant.
QT9 QMS is validated after each release, and it is in line with FDA QSRs to keep you in compliance with FDA quality system requirements.
QT9 lets you choose modules based on what's best for your organization.
With multiple modules to choose from, there's solutions for nearly anyone.
Whether you are a large corporation or a small start-up you can use as many modules as you want.
Whether you use Android, iOS or Windows, QT9 works from virtually any web browser.
Speak directly to a QT9 expert.
Have questions? Want to discuss solutions?
See a personalized demo of QT9 QMS.