Implementing the New EU Medical Devices Regulations

Posted 01 December 2017 By Randolph Fillmore

placeholder+image This article discusses the steps toward implementing the new EU regulations on medical devices with a focus on better pre-market control, establishing oversight and data systems. It is based on a presentation given by Salvatore Scalzo at the RAPS EU Regulatory Essentials Workshop held in Brussels, Belgium in July 2017.

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Categories: In vitro diagnostics, Medical Devices, Features, Europe, EC


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