By Stewart Eisenhart, Emergo Group
During the Eudamed Steering Committee meeting of December 14, 2016 the current state of play regarding the introduction of the new Medical Device Regulations (MDR) and In Vitro Diagnostic Regulations (IVDR) was presented by European Commission officials.
Get the full story here at the Emergo Group’s blog.
The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.
The post European Commission: Entry into force of MDR, IVDR set for late May 2017 appeared first on MassDevice.
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