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CLSI M23

Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters; Approved Guideline

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Organization: CLSI
Publication Date: 1 October 2008
Status: inactive
Page Count: 64
scope:

Guidelines for interpretive criteria and quality control (QC) ranges are established by the Subcommittee on Antimicrobial Susceptibility Testing after review of extensive data. This guideline describes the data needed for such determinations. The document is intended for use by the subcommittee to ensure completeness of the data on which decisions are based, and to provide guidance to sponsors of antimicrobial agents preparing presentations requesting CLSI interpretive criteria and QC ranges for newly introduced agents, or to revise these for previously reviewed agents.

Guidelines presented in this document apply only to CLSI procedures and documents. The guidelines do not apply to antimicrobial agents that are used topically or for purposes other than inhibiting the growth of or killing microorganisms.

Document History

January 1, 2018
Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters
This guideline provides direction for determining breakpoints and QC parameters for antimicrobial agents that have a direct action on microorganisms. The intended audience includes sponsors (eg,...
CLSI M23
October 1, 2008
Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters; Approved Guideline
Guidelines for interpretive criteria and quality control (QC) ranges are established by the Subcommittee on Antimicrobial Susceptibility Testing after review of extensive data. This guideline...
January 1, 1992
Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters; Tentative Guideline Second Edition
A description is not available for this item.

References

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