Special Note to PDA Members
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or Shanna Morgan
Don't miss one of the foremost technical disinfection experts walk you through the key elements of Disinfectant Validation and efficacy studies! This webinar explores three Stages: In Vitro, In-Situ and Continuous surface monitoring. Learn the challenges, variables, and complexities in Disinfectant Coupon Testing and solutions to alleviate testing issues. Both sides of the industry debate will be discussed, highlighting current: FDA, MHRA, ANVISA, ANSM, CFDA, ANMAT, and HPRA regulatory expectations while reducing the total costs for testing. A review of recommendations from PDA-TR70, Draft 12 Annex 1, and USP 43 <1072> will be covered.
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