There are many acronyms that can be used when discussing disinfectants and their validation, FDA, EPA, BPR, AOAC, EN, EU GMP, USP, ASTM the list goes on! The regulatory web can get quite confusing so an outline of the basics can be helpful. 

Life science cleanroom facilities must know that the disinfectants they are using can achieve effective levels of microbial kill across a range of surface types. 

There are many different types and formats of disinfectants now available for use within pharmaceutical cleanrooms and there are various national and international efficacy testing standards available to compare and qualify them.  

This session will help to untangle the regulatory web, understand information provided by manufacturers and select the correct disinfectant efficacy test methods to meet the requirements of GMP Annex 1 2022.

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