Disinfectant Efficacy Testing (DET) Under the Microscope: Designing Studies for Today’s Regulatory Expectations
Virtual
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Critical environments require validated disinfectants to ensure classified areas are properly maintained and compliant with EU GMP Annex 1 and other global regulatory expectations. Disinfectant efficacy testing (DET) provides scientific evidence to identify the most appropriate biocides for a given environment, enabling organizations to confidently select disinfectants and establish a robust contamination control program.
Join this complimentary webinar to learn what disinfectant validation entails and how to design and execute a DET study with confidence. Discover the critical variables that can impact study outcomes, along with key regulatory requirements and risk-based test matrix optimization strategies. Explore how STERIS’s SurePath DET Program can help your organization seamlessly implement high-performing products that strengthen your contamination control program.
Dave brings nearly three decades of professional microbiology experience, with expertise in food microbiology and aseptic manufacturing microbiology.
He holds a master’s degree in management and a bachelor’s degree in biology.
Dave has authored numerous industry publications, delivered a wide range of webinars and contributes to the advancement of industry standards. He is an active member of the British Standards Institute (BSI) CH/216 Chemical Disinfectants and Antiseptics Committee, which is responsible for European disinfectant testing standards.
Your needs are unique – so is our approach. Discover how a partnership with STERIS can reduce risk and improve sustainability and efficiency at your facility.
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