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    Live Webinars

    Product Safety: Future State of Sterility Assurance
    and the Role of Terminal Sterilization

    Register Now

    Sterilization is a pivotal step in the pharmaceutical drug development process to help ensure overall safety is maintained. Regulation is clear that, whenever possible, products intended to be sterile should be terminally sterilized in their final container. Only if terminal sterilization is not possible, filtration or aseptic assembly should be applied. This webinar will focus on trends in the concept of sterility assurance including the revision of USP 71 and elements to evaluate prior to selecting aseptic assembly for the manufacturing of sterile drug products.

    Date: December 2, 2021
    Time: 10 am EST / 4 pm CEST; 1 Hour with Q&A
    Hosted by: CPhlonline
    Speaker: Annick Gillet, Technical Director, EO Pharma, Sterigenics

    Attendees will gain a deeper understanding of:

    • Terminal sterilization and aseptic processing of drug products through a regulatory lens as well as that of a manufacturer
    • Mitigation strategies for the use of terminal sterilization with radiation, ethylene oxide and novel modalities
    • Trends in the concept of sterility assurance

    QUESTIONS

    Contact Amie Casson aecasson@sterigenics.com