Our standards for functionality, safety and reliability

Every single element of our quality management system is mapped and interlinked in a uniform database system. The comprehensive use of barcode systems and an almost fully automatic handling of the products in the context of the production and processing process up to packaging and delivery ensures that all planned individual steps are carried out, checked against each other and documented.

The comprehensive documentation of all test results, from the examination of the raw materials used to each individual production step to the release of each individual container, ensures the unrestricted traceability and safety of our products. With the help of state-of-the-art industrial image processing, we guarantee 100% control of every single part.

In order to support internationally operating customers, we maintain drug master files for selected products at the FDA and other health authorities.

Medical devices receive the CE mark on the basis of well-founded self-certifications and, if necessary, with the involvement of notified bodies.