ISO 16256:2012
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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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
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
14-10-2021
French, English, Russian
06-12-2012
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).
DevelopmentNote |
Supersedes ISO/DIS 16256. (12/2012)
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DocumentType |
Standard
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Pages |
17
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PublisherName |
International Organization for Standardization
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Status |
Withdrawn
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SupersededBy |
Standards | Relationship |
NF EN ISO 16256 : 2013 | Identical |
NBN EN ISO 16256 : 2013 | Identical |
NEN EN ISO 16256 : 2012 | Identical |
NS EN ISO 16256 : 2012 | Identical |
I.S. EN ISO 16256:2012 | Identical |
PN EN ISO 16256 : 2013 | Identical |
SN EN ISO 16256:2013 | Identical |
UNI EN ISO 16256 : 2013 | Identical |
UNE-EN ISO 16256:2013 | Identical |
BS EN ISO 16256:2012 | Identical |
EN ISO 16256:2012 | Identical |
DIN EN ISO 16256:2013-04 | Identical |
ONORM EN ISO 16256 : 2013 | Identical |
ISO 16142-2:2017 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards |
ANSI/AAMI/ISO 16142-2:2017 | MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 2: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
BS ISO 16142-2:2017 | Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards |
ASTM E 3152 : 2018 | Standard Guide for Standard Test Methods and Practices Available for Determining Antifungal Activity on Natural or Synthetic Substrates Treated with Antimicrobial Agents |
CLSI M38 A2 : 2ED 2008 | REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF FILAMENTOUS FUNGI |
CLSI M27 A3 : 3ED 2008 | REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF YEASTS |
CLSI M27 A2 : 2ED 2002 | REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF YEASTS |
CLSI M27 S3 : 3ED 2008 | REFERENCE METHOD FOR BROTH DILUTION ANTIFUNGAL SUSCEPTIBILITY TESTING OF YEASTS |
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