Establishing the efficacy of a biocide is critical to selection of the correct programme of use within any cleanroom facility.
Qualification of the efficacy of the InSpec® range is achieved via European Standards – CEN TC 216 phase 1 & phase 2 (suspension tests and surface tests). Testing was performed by accredited 3rd party laboratories.
Summary of InSpec Biocide Qualification
United States Pharmacopoeia (USP) General Chapter 1072 "Disinfectants and Antiseptics"13.
This chapter stipulates that a 3 log reduction in the viable microbial count should be demonstrated for bacteria.