What are the Clinical Laboratory Improvement Amendments commonly referred to as?

The Clinical Laboratory Improvement Amendments are commonly referred to as CLIA. This acronym stands for the legislation that governs laboratory testing and ensures the accuracy and reliability of test results. CLIA was established to regulate laboratory testing and to improve the quality of laboratory procedures and outcomes in the United States.

The focus of CLIA is to set quality standards for all laboratory testing performed on humans, which includes oversight of laboratory operations, staff qualifications, and proficiency testing. This regulatory framework is crucial for ensuring patient safety and the reliability of diagnostic testing, which is fundamental in clinical practice for diagnosing and treating medical conditions.

Other options like CLAS, CLAZ, and CLOG do not represent established terminology or acronyms associated with laboratory regulations and standards in the clinical setting. Thus, CLIA is the correct reference for the Clinical Laboratory Improvement Amendments.