Pre-validated platform
With Bizzmine, your quality processes fully comply with ISO 9001, ISO 13485, ISO 17025, ISO 15189, ISO/TS 16949, ISO 22000, 21CFR Part 11, GxP, and GAMP.
All users have easy access to the software, no matter where they work and you have full control and overview over your entire Quality Management.
It has been proved that Bizzmine is able to be qualified for use in a pharmaceutical environment.
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Get started fast
With the prebuilt processes you can implement your quality management in a couple of days.
Configure existing or new processes, without any need for coding.
Make changes yourself or count on our business consultants for help.
Go for the cloud or On-Premises. Choose for maximum comfort and security.
Scalable and flexible
Scale from a small business to a large one, spread over multiple sites. Bizzmine grows easily with your business.
Expand your digital workflow approach to other departments of your organisation.
Use Bizzmine in English, French, Dutch, German, Swedish, Portuguese, Lithuanian, or Italian. More languages can be offered upon request.
Trust our support around the globe, since we have offices on all continents.
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Audit Management
Bizzmine assists you in better organising and tracking internal and external audits.
CAPA Management
Bizzmine supports you in continuously improving the efficiency of your QMS.
Training Management
You will be able to better manage and control all training and competency data.
Complaints Management
Keep track of, investigate, and resolve customer and supplier complaints.
Calibration Management
All calibration operations can be planned, organised, and analysed.
Choose your industry to learn more
Medical Devices
See how you can implement your QMS for ISO 13485 and digitise numerous linked quality processes.
Pharma
Discover how to implement your eQMS and digitise numerous linked quality processes, according to cGMP.
Laboratories
Learn how to improve the quality and safety of your laboratory with the implementation of your eQMS.