Official, uncorrupted, and legally compliant PDF copies of M22 standards should be sourced directly from the Clinical and Laboratory Standards Institute (CLSI) official portal. Third-party document-sharing sites often host outdated, incomplete, or altered versions that can compromise lab compliance.
This section emphasizes the importance of standard precautions when performing quality control procedures using viable microorganisms, and references CDC guidelines and other NCCLS documents such as M29—Protection of Laboratory Workers.
One of the most significant contributions of the CLSI M22-A3 document is the classification of commercially prepared media into two main categories: and Non-Exempt . This classification is based on extensive multi-center studies evaluating the historical failure rates of various media types. 1. Exempt Media (Low Failure Rate) clsi m22a3 pdf
If your lab is seeking (College of American Pathologists) or complying with CLIA '88 (Clinical Laboratory Improvement Amendments), adherence to CLSI M22-A3 is considered best practice and often mandatory.
Ensure media is stored at the temperature specified by the manufacturer (usually 2°C to 8°C) and monitor storage logs. Official, uncorrupted, and legally compliant PDF copies of
Media must be stored at the manufacturer’s specified temperatures, typically between 2°C and 8°C for plates. Freezing must be strictly avoided as it destroys the agar gel matrix.
Through extensive multi-center studies, CLSI determined that certain types of commercially prepared media have exceptionally low failure rates (often less than 0.1%). Under M22-A3, if a laboratory purchases these media from a manufacturer that certifies compliance with CLSI standards, the laboratory is from performing full, routine microbial performance testing on those batches. Examples of typically exempt media include: Sheep Blood Agar (SBA) MacConkey Agar (MAC) One of the most significant contributions of the
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For non-exempt or in-house prepared media, M22-A3 outlines specific target organisms required for testing. Laboratories must use specific strains, typically sourced from the ATCC, to evaluate two primary metrics: