SS-EN-ISO-16256 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)

SS-EN-ISO-16256 - 2012 EDITION - CURRENT


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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).

To find similar documents by classification:

11.020 (Medical sciences and health care facilities in general Including quality and environmental management in health care technology IT application in health care technology, see 35.240.80)

11.100.01 (Laboratory medicine in general)

11.100.10 (In vitro diagnostic test systems)

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Designation Name

SS-EN ISO 16256:2012

Revision Level

2012 EDITION

Status

Current

Publication Date

Dec. 17, 2012

Language(s)

English

Page Count

32

International Equivalent

EN ISO 16256:2012(IDT); ISO 16256:2012(IDT)