Summary:
Ensures that medical device manufacturers are in full compliance with one of the European Directives aimed at regulating the manufacture of IVDD, MDD and AIMDD products. |
Description:
an In Vitro, regulatory affairs, IVDD, CE Mark, MDD, company for ISO and ce mark services, mdi Europa is a recognized authority for authorized european address, an authorized responsible person and authorized representative in the medical device and in-vitro device industry
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