ISO 16256:2012

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Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases

Published By	Publication Date	Number of Pages
ISO	2012-12	26

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Categories: 11.100.10 - In vitro diagnostic test systems, ISO

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Description

ISO 16256:2012 describes a method for testing the susceptibility to antifungal agents of yeasts, including Candida spp. and Cryptococcus neoformans, that cause infections. The reference method described here has not been used in studies of the yeast forms of dimorphic fungi, such as B. dermatitidis and/or H. capsulatum variety capsulatum.

ISO 16256:2012 describes the broth microdilution reference method which can be implemented by either of two pathways. One pathway involves visual determination of MICs (CLSI method); the second pathway involves spectrophotometric determination of MICs (EUCAST method).

Additional information

Published Code	ISO
Published By	International Organization for Standardization
Publication Date	2012-12
Pages Count	26
Language	English
Edition	1
File Size	297.0 KB
ICS Codes	11.100.10 - In vitro diagnostic test systems

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ISO 16256:2012

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