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Finding Reliable Clinical Laboratories In order to process human samples (like blood), laboratories must be certified to do so. The Clinical Laboratory Improvement Amendments of 1988 (CIA) regulations
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What is CLIA?
CLIA stands for the Clinical Laboratory Improvement Amendments, which are regulations that ensure the quality and accuracy of laboratory testing in the United States.
Who is required to file CLIA?
Clinical laboratories that perform tests on human specimens are required to file for CLIA certification to ensure compliance with quality standards.
How to fill out CLIA?
To fill out CLIA forms, a laboratory must complete the CLIA application, provide required documentation regarding laboratory operations, and submit fees as directed by the Centers for Medicare & Medicaid Services (CMS).
What is the purpose of CLIA?
The purpose of CLIA is to establish standards for laboratory testing to enhance the quality of laboratory services and protect public health.
What information must be reported on CLIA?
Laboratories must report information such as laboratory name, location, type of tests performed, ownership details, and compliance with quality standards as part of their CLIA application.
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