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Clinical Laboratory Improvement Amendments (CLIA)

The Clinical Laboratory Improvement Amendments (CLIA) are U.S. federal regulations that ensure the quality and accuracy of lab testing. Established in 1988, CLIA sets standards for laboratories that perform tests on human samples, such as blood and tissue. These regulations require labs to be certified and follow strict guidelines to ensure test results are reliable and safe for patient care. CLIA covers various lab types, from small clinics to large hospitals, and emphasizes ongoing quality control and assurance to protect public health.

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  • Image for Clinical Laboratory Improvement Amendments (CLIA)

    The Clinical Laboratory Improvement Amendments (CLIA) are U.S. federal regulations that ensure the quality and accuracy of laboratory testing. Established in 1988, CLIA sets standards for laboratory operations, including employee qualifications, equipment maintenance, and testing procedures. These regulations apply to all types of labs, from large hospitals to smaller facilities. By ensuring that labs meet specific requirements, CLIA helps protect public health by providing reliable test results, which are crucial for diagnosis and treatment decisions. In essence, CLIA aims to ensure that laboratory tests are safe, accurate, and effective.