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ON-DEMAND WEBINAR

ON-DEMAND WEBINAR

MDR Effects on Medical Device Processing

Published Date: August 27, 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.

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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.

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