Eight Key Steps Toward EU-MDR Implementation

Posted 13 November 2017 By Gert Bos

placeholder+image This article offers eight steps toward ensuring compliance with the new European Union Medical Device Regulations. It is based on the author's presentation given in July 2017 on "EU Regulatory Essentials, Medical Device, and In Vitro Diagnostics: Transitioning From Current Directives to new Regulations" at the RAPS Brussels Conference.1, 2

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Categories: In vitro diagnostics, Medical Devices, Submission and registration, Features, Europe, EC


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