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ON-DEMAND WEBINAR

ON-DEMAND WEBINAR

MDR Effects on Processing Devices

Published Date: May 8, 2019

The new Medical Devices Regulation (2017/745/EU) (MDR) brings EU legislation into line with technical advances, chang­es in medical science, and progress in law making.  There are many updates that effect reusable medical device manufacturers. This presentation will outline all of the testing and documentation that needs to occur prior to the MDR deadline.

Presenter: Emily Mitzel, MS

Emily Mitzel

Emily Mitzel

MS
Reusable Medical Devices Expert

Emily Mitzel is an Expert Advisor and Senior Scientist at Nelson Labs. Her expertise includes reusable device reprocessing validations, newly manufactured device validations, sterilization, and microbiology testing. Emily presents at Nelson Labs’ seminars, tradeshows, ISO, FDA, AAMI, and client facilities across the U.S. and internationally. Emily is an active committee member of many working groups...

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