We, the management of the MESO group, commit ourselves to realize an active and continuously improving quality management system (QMS).
The MESO group consistently follows stringent quality requirements to ensure a high product quality. The development of complex medical software and hardware underlies specific criterias concerning test and evaluation. During the development and test phase each step is documented and reproducible.
We continually review and enhance our QM system to improve its quality. Our corporate mission and our strict quality objectives are the basis for our daily work.
In December 2015 the MESO group has been successfully recertified.
The MESO group is certified according EN ISO 9001:2008 and medical product norm EN ISO 13485:2012.