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SRPS EN ISO 16256:2014

Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)

Oct 31, 2014
95.99   Withdrawal of Standard   Mar 31, 2022

General information

95.99     Mar 31, 2022

ISS

Z076

European Norm

11.100.10  

English  

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Scope

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).

Life cycle

NOW

WITHDRAWN
SRPS EN ISO 16256:2014
95.99 Withdrawal of Standard
Mar 31, 2022

REVISED BY

PUBLISHED
SRPS EN ISO 16256 :2022

Related project

Adopted from EN ISO 16256:2012

Adopted from ISO 16256:2012 IDENTICAL