Disinfectant Efficacy Testing (DET) Under the Microscope: Designing Studies for Today’s Regulatory Expectations
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.
Meet the Presenter
Dave Shields
Dave brings nearly three decades of professional microbiology experience, with expertise in food microbiology and aseptic manufacturing microbiology.
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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.
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