A pragmatic quality management system is the foundation of efficient product creation
The international requirements for quality management in CE marking are defined by the ISO standard EN ISO 13485 and include the prerequisites for standard-compliant development, production, implementation and maintenance of medical devices within an adequate quality management system.
We support you in the extensive challenges of development, production, installation and maintenance of your customized quality management system according to the international standard EN ISO 13485. The synopsis of the various international requirements and their integration into your company’s internal QM system are just as much a part of our specialties as the development of an expedient documentation system.
Call: +49 9123 1529250
Office adress, Visitors adress, Büroanschrift:
91233 Neunkirchen am Sand
Headquarter of be-on-Quality GmbH
Lilienstrasse 33, 91244 Reichenschwand