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STN EN ISO 16256

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Electronic version (pdc file)

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Name: STN EN ISO 16256
Validity: Valid
Number of pages: 28
Language:
EN
Paper: 14,10€
Electronic version a) Only read (without ability to print and copy) 12,69€
b) Without ability to print, with ability to copy (printscreen) 14,10€
c) With ability to print and copy (printscreen) 18,33€
Slovak title Klinické laboratórne skúšanie a diagnostické skúšobné systémy in vitro. Referenčná metóda mikroriedenia bujónu na skúšanie in vitro aktivity antimikrobiálnych činidiel proti kvasinkovým hubám pôsobiacim pri infekčných ochoreniach (ISO 16256: 2021)
English title Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021)
Release Date: 01. 01. 2022
Date of withdrawal:
ICS: 11.100.10
Sorting character/National clasification code 85 1022
Level of incorporation: idt EN ISO 16256:2021, idt ISO 16256:2021
Official Journal 12/21
Amendments
Replaced by:
Repleces: STN EN ISO 16256:2013-05 (85 1022)
Note in Official Journal:
Subject of the standard: This document 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 Blastomyces dermatitidis and/or Histoplasma capsulatum variety capsulatum. Moreover, testing filamentous fungi (moulds) introduces several additional problems in standardization not addressed by the current procedure. Those methods are beyond the scope of this document. This document describes the broth micro-dilution reference method, which can be implemented by either of two pathways. One pathway involves visual determination of MICs (CLSI method)[1][5]; the second pathway involves spectrophotometric determination of MICs (EUCAST method)[2][10].
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