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  • Clinical Laboratory Improvement Amendments (CLIA) | CMS
    The Centers for Medicare Medicaid Services (CMS) regulates all laboratory testing (except research) performed on humans in the U S through the Clinical Laboratory Improvement Amendments (CLIA) program The objective of CLIA is to ensure quality laboratory testing
  • Home | Cruise Lines International Association
    CLIA unites the global cruise industry by providing a strong collective voice for cruise lines, valuable connections and insights for Executive Partners, and training, resources, and support for the travel trade community
  • Clinical Laboratory Improvement Amendments | Clinical Laboratory . . .
    The Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations include federal standards applicable to all U S facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease
  • What is CLIA and Why It Matters for Lab Testing
    CLIA stands for Clinical Laboratory Improvement Amendments It is one of the most significant regulatory frameworks ensuring the accuracy and reliability of laboratory testing in the United States
  • Clinical Laboratory Improvement Amendments (CLIA)
    This process involves compliance with the federal Clinical Laboratory Improvement Amendments (CLIA) of 1988, which requires that all laboratories testing human specimens be certified by the federal government
  • CLIA Lookup - NPI Crosswalk
    What is CLIA? The Clinical Laboratory Improvement Amendments (CLIA) of 1988 applies to facilities or sites that test human specimens for health assessment or to diagnose, prevent, or treat disease
  • S C QCOR
    This website provides demographic information about laboratories, including CLIA number, facility name and address, where the laboratory testing is performed, the type of CLIA certificate, and the date the certificate expires
  • Clinical Laboratory Improvement Amendments - Wikipedia
    The Clinical Laboratory Improvement Amendments (CLIA) of 1988 are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, except clinical trials and basic research




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