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  • CLSI document M68 will describe validation procedures for implementing CLSI breakpoints on an antimicrobial susceptibility testing (AST) device. Guidance on validation of updated breakpoints on an AST device allows laboratories to perform testing needed for patient care while regulatory requirements ...

     08-01-2023  |  Reviewer or Advisor

  • CLSI document MM28 will provide information on clinical utility, technologies, validation, and results interpretation and reporting of oncology liquid biopsy testing. The methods and recommendations discussed in MM28 will focus primarily on detection of somatic genetic abnormalities, which are distinct ...

     10-01-2023  |  Reviewer or Advisor

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