In this webinar, you will learn about the importance of process definition (fractional) work as a part of an Ethylene Oxide (EO) validation and why it is not only important but required. The session covers topics such as relative resistance for Internal PCDs, confirming BI appropriateness, evaluating an appropriate External PCD, and calculating a D-Value to help determine an appropriate gas dwell time for the half cycle and full cycles.
Viewers will gain a comprehensive understanding of the EO validation process, including the steps involved in defining and validating the sterilization process. The webinar emphasizes the importance of selecting the appropriate process parameters and ensuring that the validation activities are thorough and compliant with industry standards.
By viewing this webinar, professionals involved in quality assurance, process validation, and sterilization will gain valuable insights into the EO validation process. This knowledge will help them ensure that their sterilization processes are effective, reliable, and compliant with regulatory requirements. The session will also provide practical guidance on how to optimize the EO sterilization process to achieve the desired Sterility Assurance Level (SAL).