In this white paper, we explore options for conformity assessment routes under the EU Medical Devices Regulation (MDR 2017/745).
European medical device compliance under the Medical Devices Regulation (MDR) will mean new conformity assessment route options. For medical devices that require NB involvement, a manufacturer may choose between different modules to demonstrate compliance and obtain CE Marking. If you plan to pursue CE Marking under the MDR, it's important to understand how conformity assessment routes will change as compared to the MDD.
In this white paper, we discuss some options, or differences, in selecting a route to conformity assessment for a particular device, including:
Download this paper for a practical guide to conformity assessment options under the MDR.
Since the publication of ISO 13485:2016, risk management is a major concern for maintaining regulatory compliance in major medical device markets.
read moreThe experts from Emergo by UL’s Human Factors Research & Design (HFR&D) team will share insights learned from creating a safe setting to co
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