EU MDR 2017/745: Optimizing Clinical Evaluation Reports within the Medical Device Lifecycle

MessageThis Webinar is over
Date Aug 7, 2018
Time 2-3 pm
Cost Free
Online
Free webinar-online 

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.

 


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