Human experience for technical perfection
For us, quality is the most important part of our requirements for our products and services. Within this framework, we meet the requirements of the ISO 13485:2021 standard, the MDR 2017/745 and the EEC Directive 93/42 with regard to the applicable transition periods.
We combine experience and know-how regarding automated production processes in order to be able toproduce medical precision products for you. In order to be able to meet these quality requirements also in the future, we are continuing to expand our quality assurance system in line with the ever-increasing requirements.
Regular employee trainings ensure an extremely high level of skill and knowledge. This is also extraordinarily important to us. This is due to the fact that even in a highly regulated environment, every single employee bears enormous responsibility.