Late last year, the International Organization for Standardization (ISO) standard for ethylene oxide (EtO) sterilization residuals was published. The standard uses health-based risk assessment to establish limits. The standard also includes analytical procedures for determining residue levels in devices that have been validated through interlaboratory evaluation.
CITATION STYLE
Page, B. (1996). Sterilization. Medical Device and Diagnostic Industry, 18(6), 68–73. https://doi.org/10.1093/innovait/inn071
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