21 CFR Part 211 compliance made simple.

21 CFR Part 211 compliance software for pharmaceutical companies is included with QT9™ QMS. Easily meet FDA regulations accurately and efficiently with an easy-to-use quality management system.

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21 CFR Part 211 modernization for the modern pharmaceutical company.

Keep track of pharmaceutical compliance items and synchronize documentation with anyone, anywhere.

Track all your 21 CFR Part 211 information in one place.

QT9's easy-to-use 21 CFR Part 211 system makes pharmaceutical traceability and transparency simple.

Built-In Dashboard

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.

Electronic Signatures

Make approvals electronically with electronic signature capturing built-in. QT9's 21 CFR Part 211 quality management system is 21 CFR Part 11 compliant.

Software Validation

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™ QMS is flexible for your business.

QT9 lets you choose modules based on what's best for your organization.

Modules for any business size

With multiple modules to choose from, there's solutions for nearly anyone.

A solution that scales with you

Whether you are a large corporation or a small start-up you can use as many modules as you want.

Cross-Platform Support

Whether you use Android, iOS or Windows, QT9 works from virtually any web browser.

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