ISO 13485 is the internationally recognized standard for quality management in the medical device industry.
At DEKRA, we have hosted webinars about this topic to inform customers about the transition to the IVDR.
65 58119 Hagen-Hohenlimburg Tel.
Canada - CMDR• Die.
The Medical Device Single Audit Program MDSAP is designed to allow a single audit for medical device manufacturers that is accepted in multiple countries.
Feuerwehr Hagen, Hagen.
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