Harmonised Standards unter the MDR -- MEDICA - World Forum for Medicine

10.09.2019

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Harmonised Standards unter the MDR

The European authorities and institutions still have to work elaborately on the harmonisation of standards under the Medical Device and In-Vitro-Diagnostics Regulation. Before we try to provide a prospect on further instruments for proof of compliance, we first would like to answer the question of what harmonised standards are and why they are necessary. Also, what recommendations for action apply to manufacturers of medical devices in the current situation, some of which have not yet been clarified.

Exhibitor Data Sheet