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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
- 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
- Clinical Laboratory Improvement Amendments (CLIA) | FDA
This page contains information about The Clinical Laboratory Improvement Amendments (CLIA) that regulate laboratory testing
- CLIA | HHS. gov
Under the HIPAA Privacy Rule, patients, patient’s designees and patient’s personal representatives can see or be given a copy of the patient’s protected health information, including an electronic copy, with limited exceptions
- 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
- CMS’s CLIA Rule Now Fully in Effect - ascp. org
On December 28, 2024, the Centers for Medicare Medicaid Services’ (CMS) final rule updating the Clinical Laboratory Improvement Amendments regulations went fully into effect
- 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
- MLN006270 CLIA Program Medicare Lab Services - HHS. gov
Through the Clinical Laboratory Improvement Amendments (CLIA) Program, CMS regulates all lab testing (with some specific exceptions and state exemptions) done on humans in the U S to ensure accurate, reliable, and timely patient test results
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