ISO 13485:2003 CMDCAS
Liofilchem's Quality Management System is certified by Tüv Süd America Inc. for design and development, production and sale of in-vitro diagnostic medical devices.
UNI EN ISO 9001:2008
Since 1997 the implementation of the Quality System Management permits to satisfy Customer expectations, optimize resources, qualify and consolidate the company position in national and international market.
UNI EN ISO 13485:2012
Liofilchem manufactures In Vitro Medical Diagnostic Devices conform to the use destination provided for and current regulation requirements.