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hi everyone and welcome to todays webinar guidance for cleaning disinfection and sterilization of reusable medical devices I am pleased to introduce todays speakers mehdi sahara and stephanie of Aswath both Stephanie and Melissa have been working for several years in our microbiology lab and have a lot of experience in microbial testing in vitro toxicology testing and reprocessing validations I now hand the microphone over to Melissa Thank You Katrina and thank you for the nice introduction you probably noticed that the new medical device regulation was published by European authorities which has of course some major changes as compared to previous regulatory documents that existed for medical device manufacturers in this webinar Stephanie and I will highlight the important points that are addressed to processing of reusable medical instruments you will also get inside in the design of processing validation studies as you probably already know the current European medical device dire
