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Mike PadillaSenior Manager, EO ConsultingSteriPro Consulting

Mike Padilla joined Sterigenics International in 1997 (formerly Griffith MicroScience) as Corporate Quality Engineer and in 2000 joined SteriPro Consulting. In his current position, he is responsible for leading the SteriPro EO Consulting team in the development and management of ISO- and FDA-compliant sterilization studies including Process Definition, Cycle Validations, Parametric Release and Cycle Optimization for ethylene oxide processing. Mike is also a presenter at the Annual SteriPro Sterilization Seminars given to the medical device and pharmaceutical industries. Prior to joining Sterigenics, Mike served a total of 6 years between Baxter Healthcare and Allegiance Healthcare where he managed various projects ranging from both product development and validation in Steam and Ethylene Oxide sterilization modalities. He is an active member of ISO/AAMI/TC 198 where he serves as a working group member of WG01, Industrial EO Sterilization, including member of the AAMI Process Equivalency Task Group which developed TIR 28, Product Adoption and Process Equivalency for Ethylene Oxide Sterilization.

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