Paperless production with modern MES software - GxP compliant

For 18 years, DOQ has been meeting all the demands made in the healthcare sector on modern software for generating an eDHR (electronic Device History Record) with MES functionalities.

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

DOQ can be introduced within only 3 months due to its modern interface architecture and high user acceptance. We support you with all the necessary training and documents needed for going 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.