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Automate your 21 CFR Part 211 compliance processes with the cloud-based QT9 QMS solution.
Easily manage 21 CFR Part 211 compliance items with anyone, anywhere.
QT9 QMS reduces staff time by eliminating manual processes.
Meet FDA regulatory requirements for pharmaceuticals.
Centrally upload, publish & distribute documents.
Meet Current Good Manufacturing Practice (CGMP) with ease.
The QT9 QMS is your all-in-one 21 CFR Part 211 software solution.
QT9™ QMS Management Review Module
QT9™ QMS Audit Management Module
QT9™ QMS Employee Training Module
QT9™ QMS Engineering Change Request Module
QT9™ QMS Document Control Module
QT9™ QMS Supplier Evaluation Module
QT9™ QMS Inspection Module
QT9™ QMS Calibration Module
QT9™ QMS Nonconforming Product Module
QT9™ QMS Corrective Actions Module
QT9™ QMS Customer Feedback Module
QT9™ QMS Risk Assessment Module
QT9's easy-to-use 21 CFR Part 211 system makes pharmaceutical traceability and transparency simple.
Quickly see the status of 21 CFR Part 211 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 21 CFR Part 211 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.