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CLIA means Clinical Laboratory Improvement Amendments.
CLIA for medical abbreviation means "Clinical Laboratory Improvement Act".
The Clinical Laboratory Improvement Amendments (CLIA) is a federal law in the United States that promotes accuracy in medical laboratories by establishing quality standards for laboratory testing to ensure the reliability and accuracy of patient test results.CLIA establishes quality standards for laboratory testing to ensure the accuracy, reliability, and timeliness of patient test results.
Clia
Clinical laboratories that perform testing on human specimens for the purpose of diagnosing, preventing, or treating diseases must abide by CLIA regulations set by the Centers for Medicare & Medicaid Services (CMS). These regulations are in place to ensure the accuracy, reliability, and timeliness of clinical laboratory test results.
CLIA waived tests are simple laboratory tests categorized as low-risk for incorrect results. They are considered easy to perform with minimal chances of errors when conducted correctly, and therefore do not require stringent laboratory personnel qualifications or extensive quality control measures under the Clinical Laboratory Improvement Amendments (CLIA) regulations in the United States.
The Dept. of Labor's Occupation Safety & Health Administration (OSHA) is responsible for laboratory workplace safety in those states with direct federal authority for occupational safety and health, and in those laboratory containing institutions not subject to Department of Energy safety authority.
CLIAClinical Laboratory Improvement Amendments
Diagnosis is achieved first by a clinical diagnosis from a clinical geneticist, followed by molecular genetic testing in a CLIA-approved diagnostic laboratory
Swiss Gemological Laboratory
IN 1988
36415 is the code for the venipuncture; it does not describe a particular test, so it is not regulated by CLIA.