Paperless production with modern MES software - GxP compliant

For 18 years, DOQ has met all the requirements placed on modern MES software in the healthcare sector .

What advantages does DOQ offer you?

Regulatory Compliance

As a quality-relevant and regulatory correct MES solution, DOQ bears the main burden of validation and collects quality-relevant data from all other systems, which are integrated in compliance with FDA 21 CFR Part 11. With this company-wide approach, you ensure the long-term validity and compliance of all software systems used.

Short implementation phase

Thanks to its modern interface architecture, DOQ can be implemented within only 2 months. This already includes all the necessary training courses and documents that you need to go live.

What functions does DOQ offer you?

Data analysis

All existing database entries can be evaluated time-controlled or across process chains and visualized in individual dashboards.


Traceability within seconds and focusing on all existing predecessors enables unrestricted tracking and tracing in vertical and horizontal levels.

Our Support

System introduction and validation

When introducing DOQ MES we support you with all relevant documentation up to the IQ-OQ-PQ documents. The corresponding test sequences then form the conclusion of the validation.


The installation and data storage can be realized both on own servers and as a cloud based solution. The well thought-out role/user concept can be individually adjusted to all needs and also allows DOQ to be used across multiple locations.
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