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PDF M52 Verification of Commercial Microbial Identification and

Clinical and Laboratory Standards Institute document M52—Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems provides recommendations for verification of commercial US Food and Drug

PDF Verification of Commercial Microbial Identification and

Clinical and Laboratory Standards Institute document M52—Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems provides recommendations for verification of commercial US Food and Drug

  • What is M52 validation?

    In order to align M52 with globally harmonized terminology, validation is the term used to describe the process that manufacturers follow to set test performance specifications.

  • How long after reaffirmation is a m52-ed1 reaffirmed?

    The document’s next scheduled review is generally five years after the reaffirmation date. You may also be interested in... Buy M52-Ed1, “Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems,” at CLSI. View Microbiology standards.

  • What is CLSI document M52 1?

    CLSI document M52 1 describes a detailed protocol on Verification of commercial microbial identification and antimicrobial susceptibility testing systems. What is required to be tested for an antimicrobial susceptibility testing (AST) system verification? 1,2 Accuracy and precision are the main performance specifications:

  • What does “must” mean in M52?

    Throughout M52, the use of the term “must” was evaluated by the document development committee and deemed appropriate because the uses are either 1) based on a requirement or 2) indicative of a necessary step to ensure patient safety or proper fulfillment of a procedure.

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