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The M22 document outlines the quality control (QC) procedures for commercially prepared microbiological culture media, serving as an essential standard for both media manufacturers and clinical laboratory users. The fundamental premise of the M22 standard is that rigorous, routine retesting of commercially prepared media by the clinical laboratory is often redundant and unnecessary, provided the media comes from a reliable source.
Media with a proven track record of high stability and exceptionally low failure rates when produced under stringent manufacturer QC. clsi m22a3 pdf link
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Manufacturers must provide a Certificate of Analysis (CoA) to prove this testing occurred. 2. User (Laboratory) Responsibilities Media with a proven track record of high
The provides a roadmap for the quality control (QC) of commercially prepared microbiological culture media. It covers:
Information about the standard is available through technical standard repositories like GlobalSpec . Importance of Using the Correct Standard
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