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Webinar: EU MDR 2017/745: Optimizing Clinical Evaluation Reports Within the Medical Device Lifecycle
August 7, 2018 @ 10:00 am - 11:00 am
As there are less than two years remaining prior to the MDR enforcement, it is critical that EU device manufacturers prepare now for conformity by May 2020.
In this webinar, NAMSA’s Manager of Medical Writing and Regulatory Services (EMEA), will examine the requirements listed in the MDR and MEDDEV 2.7/1 Rev 4, and discuss why device manufacturers shall not consider the CER a mandatory document for NBs or authorities, but rather as a crucial tool for a smooth transition for MDR and beyond.
Time will also be allotted for Q&A.