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  • Clinical Laboratory Improvement Amendments
    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
  • Test Complexities | Clinical Laboratory Improvement Amendments (CLIA) | CDC
    Clinical laboratory test systems are assigned a moderate or high complexity category on the basis of seven criteria given in the Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations
  • Documents | Clinical Laboratory Improvement Amendments (CLIA) | CDC
    Find Clinical Laboratory Improvement Amendments of 1988 (CLIA)-related documents in the Federal Register and Code of Federal Regulations
  • Provider-Performed Microscopy Procedures | Laboratory Quality | CDC
    Find educational materials and other helpful resources for the Clinical Laboratory Improvement Amendments (CLIA) Certificate for Provider-Performed Microscopy (PPM) procedures
  • CLIA Proficiency Testing Final Rule
    This final rule implements revised regulations that the Centers for Medicare Medicaid Services (CMS) and the Centers for Disease Control and Prevention (CDC) proposed in 2019 to update CLIA PT regulations
  • Waived Tests | Laboratory Quality | CDC
    United States lab facilities are regulated under Clinical Laboratory Improvement Amendments of 1988 (CLIA), including waived tests These tests must be performed correctly to avoid errors and serious health impacts
  • CLIA Certificates | CDC Laboratories
    CDC laboratories that perform clinical testing (except clinical trials and basic research) must adhere to Clinical Laboratory Improvement Amendments (CLIA) requirements and maintain current certification of CLIA compliance
  • CLIA Laboratory Search - CDC
    Select “CLIA Laboratory Lookup” under “Tool” in the left-hand navigation Please email CMS directly at LabExcellence@cms hhs gov for inquiries about data in their lookup


















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