Clean room

Medical/pharmaceutical products and/or packaging are produced to high standards of cleanliness under clean room conditions. The installation conforms to standard ISO-7 per DIN EN ISO 14644-1 and GMP Classe C. The ISO 13485 standard represents the specific requirements for our quality management system in the field of medical devices.

The production lines are equipped with inspection cameras for strip of film and are regularly requalified by external partners.