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Quality - Accreditation - Certification

GBA MDS - DIN EN ISO/IEC 17025, Medical Device Regulation (MDR), GLP

DIN EN ISO/IEC 17025, Medical Device Regulation (MDR), GLP

Quality is the basis of our services, and an essential factor to inspire your confidence in our work.

GBA Medical Device Services is accredited (with ILAC Mutual Recognition Arrangement) for biological, microbiological and hygiene testing according to DIN EN ISO/IEC 17025 (for medical devices) by the Deutsche Akkreditierungsstelle (German Accreditation Body) (DAkkS, D-PL-13392-01)

Certificate DIN EN ISO/IEC 17025

Translation DIN EN ISO/IEC 17025

Scope DIN EN ISO/IEC 17025

Normative Background ISO 17664

GBA Medical Device Services is GLP (Good Laboratory Practice) certified by the Bayerische Überwachungsbehörde (Bavarian supervisory authority)

Certificate GLP

GLP certified

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