By Stewart Eisenhart, Emergo Group
The European Commission has clarified its designation process for appointing expert panels to support regulators, Notified Bodies and other entities meet requirements and obligations of the Medical Devices Regulation (MDR) and In-vitro Diagnostic Medical Devices Regulation (IVDR).
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 DrugDeliveryBusiness.com or its employees.