Why Should You Attend:
R&D Engineers have the responsibility of the development of medical devices or healthcare products that will be sterilized by ethylene oxide (EO), however they may not have an adequate understanding of the sterilization process and its impact to the functionality of the product and its package. This presentation will provide information that can be used by R&D Engineers to aid them in the selection of materials, design characteristics and appropriate packaging by providing them with a basic knowledge of what is involved in the process of EO sterilization. It will also provide guidance on how the EO sterilization process can be changed to address specific product needs such as temperature or moisture sensitivity.
Areas Covered in the Webinar:
Who Will Benefit:
This webinar will provide valuable information to companies that design products for terminal sterilization with ethylene oxide.
Gerry O’Dell, is owner and President of Gerry O’Dell Consulting, a consulting firm based in the United States with medical device and pharmaceutical clients around the world. Her over 35 years of experience in all the major sterilization methods, microbiology, environmental control, laboratory compliance, failure investigation, has enabled Gerry to successfully consult to companies ranging from small start-up operations to Fortune 500 companies. She has also played a significant role in sterilization standards development for over 25 years through her association with the American Association for the Advancement of Medical Instrumentation (AAMI).
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