Courtesy of Meredith M. Hackel, International Health Management Associates. Used with permission. CLSI standard M Reproducibility of broth microdilution MICs for the novel siderophore cephalosporin, cefiderocol, determined using iron-depleted cation-adjusted Mueller-Hinton broth. Diagn Microbiol Infect Dis. The cefiderocol concentrations in wells A1 to A12 are 0. Row A shows the cefiderocol MIC at 0. The growth control well is B11 black box.
This page is intentionally left blank. Glossary I In the late s, several authorities were consulted to construct the glossary. The intention was to include all agents that appeared in M, along with related agents available for human use.
Since that time, agents have been added to the glossary as they were introduced to CLSI, and they do not need to be FDA cleared to be included. It cannot be assumed that the list is exhaustive, and it should be noted that some agents are no longer available for human use.
Footnotes a. Hydrolyzed by staphylococcal penicillinase. Not hydrolyzed by staphylococcal penicillinase. Glossary I M, 30th ed. Glossary II In the late s, several authorities were consulted to construct the glossary. Continued Footnotes a. Abbreviations assigned to one or more diagnostic products in the United States. If no diagnostic product is available, abbreviation is that of the manufacturer. As available in the United States. Amikacin-fosfomycin is aerosolized and inhaled. Glossary III In the late s, several authorities were consulted to construct the glossary.
For Use With M02 and M07 The Quality Management System Approach Clinical and Laboratory Standards Institute CLSI subscribes to a quality management system QMS approach in the development of standards and guidelines that facilitates project management, defines a document structure using a template, and provides a process to identify needed documents.
A laboratory path of workflow consists of the sequential processes: preexamination, examination, and postexamination and their respective sequential subprocesses.
All laboratories follow these processes to deliver their services, namely quality laboratory information. Continuing without changing cookie settings assumes you consent to our use of cookies on this device. You can change these settings at any time, but that may impair functionality on our websites. Review our privacy policy. Access Our Free Resources. Free Susceptibility Testing Resources. CLSI documents undergo periodic evaluation and revision to keep pace with advances in technology. Procedures, methods and protocols affecting laboratory or healthcare.
At the end of each comment period in the review and comment process, the committee was formed. The document is required to review all comments, respond in writing to all basic comments, and review. Draft document appropriate Comments on published CLSI documents are equally important and can be submitted by anyone, at any time. A document All comments are organized by a committee of experts following a consensus process. When it is assumed that an objection has not been properly considered and answered, action is taken.
CLSI standards are followed by documented appeals in development policies and procedures. Download M23S. Download EP This report provides a standardized symbology for use throughout CLSI documents. Get helpful, affordable training with on-demand webinars.
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