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    Resources

    Ethylene Oxide

    Optimizing Ethylene Oxide Sterilization: Sustainable Solutions for Pharmaceutical Packaging and Drug Delivery Devices

    Ethylene oxide (EO) remains the sterilization method of choice for approximately 50% of all single-use medical devices worldwide...

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    Sustaining the Continued Safe Use
    of EO: Cycle Design and Optimization

    Join us for an insightful webinar on Sterigenics' ongoing efforts and commitment to sustaining the continued safe use Ethylene Oxide (EO) sterilization, through its global initiative...

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    The 3Rs of EO Sterilization: Sustaining the Continued Safe Use of Ethylene Oxide

    Ethylene Oxide (EO) sterilization technology plays a vital role in enabling critical medical products...

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    Product Adoption for Ethylene Oxide Sterilization

    Adoption of a new product into a device family or changes to the design and...

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    EO Sterilization: Considerations for Neonate Products and Medical Devices & ISO 10993-7

    EO sterilized items are life-saving and critical devices that are sterilized in highly regulated environment…

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    Part 2: Validating, Optimizing and Monitoring EO Sterilization Processes

    Establishing an EO sterilization process can be a complicated path as multiple factors play a role in the design of...

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    Part 1: Validating, Optimizing and Monitoring EO Sterilization Processes

    Establishing an EO sterilization process can be a complicated path as multiple factors play a role in the design of...

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    Why is the sterility of your drug product much more than just a test of sterility?

    A lack of sterility and sterility assurance continue to be a significant reason for drug recalls and regulatory citations and...

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    Key Elements of a Sterility Assurance Program

    This presentation will provide aspects of a sterility assurance program for a pharmaceutical product. Sterility assurance begins at the early…

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    Process Definition – The Critical First Steps in the Validation of an EO Sterilization Process

    In this course, you will learn about the importance of process definition (fractional) work as a part of an EO validation and why it is not only important but required.

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