Digital QMS in Healthcare 

Bizzmine dramatically reduces your time to manage and run clinical audits and other compliance activities within your departments.

An eQMS in healthcare can significantly improve overall quality, safety, and compliance while also enhancing operational efficiency and cost-effectiveness.

The software will manage clinical governance in departments such as: Pharmaceutical (GMP / MHRA Compliance), Pathology  (ISO 15189, ISO 22870), Radiology (QSI), including other departments such as Blood and other ISO’s.

Implementing a Quality Management System helps you to organize and link numerous processes:

- Clinical Audits and Audit Schedules

- Document Control, Document Changes, Training and Exams

- Non-Conformances, Positive Events and Deviations

- CAPA (Corrective Actions & Preventative Actions)

- Change Control and Equipment Management

- Risk Management

- Supplier Management


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Some of the commonly asked eQMS Features


Validation templates

We can provide validation template of core modules and processes to ensure you are fully compliant.


Digital signatures

Bizzmine is fully FDA CFR Part 11 compliant and offers digital signatures for full traceability.


Risk registers

Risk is an integral part of eQMS. From any area of the system a risk can be registered or maintained.


Mobile access

Register deviations and actions, access documents or use any other part of the system from your mobile phone or tablet.


Browser based

Nothing to install, all access is via a web browser. You have full browser choice: Firefox, Chrome, Internet Explorer & Microsoft Edge.


Reminders and deadlines

All steps within a process can have custom deadlines that issue reminders for users and escalation to managers.

You are in good company

15 key Digital QMS essentials for the Healthcare
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With BizzMine you have validated QMS software according to GAMP5 standards.

These certifications can help you improve overall performance, eliminate uncertainty, and widen market opportunities.

The validation of your Quality Management System can be easy if you rely on our eQMS prebuilt validated processes.

And as your business grows, so must your quality management. A digital QMS can scale to meet increasing documentation, processes and requirements.

The BizzMine workflow module has made our CAPA and MoC processes ‘paperless’ and compliant with the requirements of 21 CFR Part 11.

15 requirements you need to find in a solid digital QMS
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Audit Management

Bizzmine helps you to better organize and follow up your internal and external audits.

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CAPA Management

Bizzmine helps you to continually improve the effectiveness of your QMS.

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Training Management

Bizzmine helps you to better manage and control all data on training and competencies.

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Complaints Management

Track, investigate, and correct your customer and supplier complaints. 

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Calibration Management

Bizzmine is the perfect application to plan, organize and analyze all calibration processes.

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Document Control

Centralized management of SOPs, manuals, work instructions and other documents.