Our expertise
We have many years of experience in auditing quality management systems according to European and international requirements, as well as in the evaluation of technical documentation.
Above all, our aim is to make a major contribution to making your medical products safer and to sensitise you to align and optimise your processes accordingly.
Appropriate lean management, including the corresponding tools, can also have positive effects on process costs.
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Training

Implementation of training for the following courses:
- Internal Auditor
- Medical Device Regulation - MDR 2017/745
- Qualitätsmanagement Auditor (QMA)
- Medical Device Single Audit Program - MDSAP
- Market Approvals for the Brazilian, Canadian, Australian and US markets
Do you have any further questions?
We will be happy to answer them!
Use our practical contact form or call us now without obligation at +49 1525 846 12 75. We will also be happy to advise you directly on site.