Learn from our experts
Register to learn about chlorine dioxide gas sterilization, including technical, validation, and lifecycle considerations for medical devices.
As medical device manufacturers evaluate available sterilization modalities, chlorine dioxide gas is receiving increased attention as a potential option for certain products and applications. Join speakers from ClorDiSys and TÜV SÜD for an educational discussion covering the scientific principles of chlorine dioxide gas sterilization, general validation considerations, publicly available regulatory requirements, and factors associated with its use.
This webinar will provide a broad overview of the technical, validation, material compatibility, and regulatory considerations manufacturers should consider when evaluating chlorine dioxide gas sterilization for new and existing products.
What you'll learn
Understanding chlorine dioxide gas sterilization
Explore the science and technology of chlorine dioxide gas sterilization, including its advantages, limitations, and potential medical device applications.
Validation and regulatory considerations
Learn key validation requirements, regulatory expectations, and common considerations when evaluating this sterilization modality.
Material compatibility and product applications
Explore material and packaging compatibility considerations for chlorine dioxide gas sterilization of new and existing medical devices.
Who should attend
This webinar is designed for professionals involved in medical device development, sterilization, validation, quality, and regulatory compliance. It will be particularly valuable for organizations evaluating alternative sterilization methods or seeking a deeper understanding of chlorine dioxide gas sterilization technology.
• Medical device manufacturers and OEMs
• Regulatory affairs and quality professionals
• R&D teams and product development stakeholders
Meet the speakers
Emily Lorcheim, MBA, PMP
Vice President, Sterilization Technologies, ClorDiSys
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