EO sterilized items are life-saving and critical devices that are sterilized in highly regulated environment, under strict normative rules and with the greatest care.
This webinar will review important considerations for EO Sterilization of neonate products and medical devices. Aspects of EO sterilization will be covered, including the consideration for EO residues that takes into account the amendment of the governing standard, ISO 10993-7. The use of risk assessment, risk/benefit evaluation, validation and application of the right method to define the most suitable limits will also be discussed during this webinar.
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