- Document Control
- Hazardous substances
Corrective and Preventive Action Management helps you continuously improve the effectiveness of your quality management system. Launch and link actions from any other process and monitor your CAPA data through your dashboards. Plan, Do, Check & Act.
Audit Management helps you track your internal and external audits and have easy access to the audit process. Capture all relevant data in the customizable audit form and initiate corrective actions (CAPA). The intuitive workflow process is monitored with deadlines.
Manage your documents in a structured way and rely on a fully compliant version control. Centralize the management of your standard operating procedures (SOPs), manuals, documentation, work instructions, and other documents.
Track, investigate, and correct your customer complaints, supplier complaints, and internal deviations.
Calibration Management allows you to schedule all your calibration processes and get reminder notifications of deadlines.
The Training Management module allows you to centralize and control all data on training and competencies in your organization.
The VARIO Incident Management module allows you to take a proactive approach to safety in your business, based on accurate records, in-depth investigations, and targeted prevention.
The VARIO Inspections & Surveys module lets you implement a streamlined approach to managing inspections and audits.
The VARIO Materials Management module is a streamlined way to manage and maintain your equipment and ensures that your company meets regulatory and operational requirements.
The VARIO Risk Management module lets you manage risks properly and reduce the risk of accidents and operational disruptions.
With the VARIO Hazardous substances module, you can perfectly manage and control all hazardous substances and related safety measures.
Our QHSE Management software is easy to set up,
without technical knowledge, works on all devices, and is available in the Cloud or On-Premises.
Improve your organization’s productivity by 64% on average.
Save up to 67% on your paper budget.
BizzMine relieves you from 95% of all validation activities.
Cloud or On-premises
Cloud or On-premises?
Choose for maximum comfort and security.
Get up and running in a couple of days with the prebuilt processes.
Configure existing or new processes, without any coding.
Scale from a small business to
a large one, spread over
Easy access for all employees, wherever they work, on all screens.
Trust our support around
the globe, we have offices
in all continents.
We love the flexibility of the system and custom form collections, which gives us the option to replace all manual Word and Excel sheets we are still using today.
Michiel Pauwels, IT & Digital
The validated BizzMine platform and our user-specific applications within the software can perfectly be used in a pharmaceutical environment.
Jeroen de Jong, Manager QHSE
If you start your day with BizzMine and you follow the correct procedure, there is no way you can go on working with a wrong or outdated document.
Lynn Ackermans, Team Leader Logistics
Jurgen De Beer, Quality Administrator
BizzMine is easy to set up and user-friendly for the user organization.
Paul van der Tholen, Group IT Manager
ZINQ chose to implement the BizzMine Software because it offers a fully compliant document management system that meets all the requirements of our ISO standards.
Dory Thijs, Executive & Purchase Assistant
BizzMine is a great tool for quality management. You can record exactly what is expected from your employees, and you know the status of each registration at any time. This gives you the perfect data for statistics.
Bram Lammens, Quality Manager and Prevention Advisor
Sylphar has chosen BizzMine because of its intuitive approach and the wide range of possibilities.
Koen Steyaert, Chief Operating Officer