Highly qualified, motivated and responsible staffs are the guarantor of the development and production of innovative and reliable medical devices. Therefore, processes and procedures set out in writing as well as regular trainings are essential.

Internationally recognized licenses ensure worldwide sales of our products. Since 1995 the quality management system of IBA Dosimetry is certified and continuously adapts to changing requirements. Nowadays the quality management system meets the regulations of DIN EN ISO 13485:2003 and is supervised by DEKRA as a notified body as well as by internal audits.

In line with the quality management system, IBA Dosimetry additionally implements the demands of the American „Quality System Regulations“(QSR) and the Canadian „Medical Device Regulations“(MDR).

Due to the permanent development of the quality philosophy, a constant improvement of service and organisation is carried out.