Upon Our Word | Certified Quality Management

KLS Martin has implemented a total quality management system certified according to DIN EN ISO 13485, DIN EN ISO 9001 and the European legislation concerning medical devices. Of course, relevant national regulations have been taken into account as well - such as the requirements of the United States Food and Drug Administration (FDA), Health Canada, and the regulatory bodies of all countries throughout the world where KLS Martin Group products may be supplied.

This ensures that all our products are consistently checked in a controlled process until they are finally released after thorough testing and inspection (100% quality check). Rigorous quality control is supported by analyses and materials testing conducted in our own high-tech lab, as well as independent institutes before launching them on the market.

Any insight gained from deviations and complaints is fed into a continuous quality optimization process to make sure that our products steadily improve. Better for users - and better for the application at hand.