PolyVation was audited in November 2024 for certificate renewal of its ISO 13485:2016 quality management system. The extensive audit by DEKRA took over 3 full days. We again passed the audit with great success and received the certificate. PolyVation is certified for compliance with the ISO 13485:2016 standard with the scope: "Design and development, analysis, testing and custom manufacturing of polymers for medical and pharmaceutical applications". We are very proud to be certified for ISO 13485 since already 2010 and to be one of the first biomaterial companies in the world with such certification for such a long time. Quality is a process of continuous improvement, and this illustrates the high level at which we operate. We believe that quality is instrumental in getting groundbreaking innovations in medicine to the patient and this is what drives us each day.

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