Manage your GxP processes in good quality with QMex's advanced features and modules.

What is QMex

It is a software designed modularly for the purpose of operating GxP processes electronically, which can be integrated in each module and other corporate applications, comply with 21 CFR Part 11 requirements and facilitates compliance with legal requirements that is accessed via internet browsers and validated according to GAMP 5.

Powerful and safe key features of QMex


Data security is one of the key features of QMex. QMex has gained the trust of the market for years. Complies with 21 CFR Part 11 requirements.


QMex is a ready-to-use product, it can be used immediately after the parameters are defined and validated after the installation. However, if desired, it can be customized according to your GxP processes.


As the data grows, it does not decrease performance, all functions work stably.


Validated according to GAMP 5. Validation documentation can be shared.


Optionally, it can be licensed as cloud or on-premises.

QMex functions that make your job easier

Electronic signature
System and module based authorization
LDAP integration
Audit Trail
Registry history
Action-based and automated timely notifications
Personal Page: Pending Jobs, Delegated Jobs, Bookmarks
Graphic reporting
Trend reports
Validated reports
Printer-friendly versions of records
Configuration screens
Add multiple files
The Related Records screen, which allows you to view the records associated with each other
Multiple location support
Multi language support
Different reporting and sorting options
Integration between modules
Integration into all 3rd party software including ERPs
Powerful workflow management
User-friendly interfaces

Some of the processes we carry to the electronic environment on the QMex platform

Change Control Management
Non-Conformance Management
CAPA Management
Complaint Management
Document Management
MBR Control & Printing Management
Training Management
Audits and Inspection (Internal, External, Supplier) Management
Analytical Result Assessment (OoS / OoT) Management
Product Quality Review Management
Artwork Management
Risk Management
Pharmacovigilance (Adverse Reaction) Management
Supplier Qualification Management