| Bioteck® adopts a rigorous, functional quality system that guarantees extremely high standards throughout the production process, from receipt of raw materials through to delivery of the finished product..
Bioteck® also meets customer demands, evaluates customer satisfaction, and listens to the customer's needs through tested procedures that are monitored and functional, and which allow the company to manage the requests and suggestions received in a very punctual manner.
Maintenance, year after year, of these high quality parameters, is certified by CSQ and CSQ-MED. The latter specifically concerns companies working in the medical field. The Bioteck® quality system complies with standards ISO 9001:2000 and ISO 13485:2003, specific for the quality management of medical devices.
Bioteck® bone substitutes are medical devices that comply with the most recent European standards of reference, as certified by the CE marking released by the Istituto Superiore di Sanità, Notified Body no. 0373.
You can view or download the certificates directly by clicking on the images.
 
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