Standards and Certification: Laboratory Requirements (42 CFR 493)external icon Show The section of the federal regulations titled “Standards and Certification: Laboratory Requirements” is issued by the Centers for Medicare & Medicaid Services (CMS) to enact the CLIA law passed by Congress (see below). In general terms, the CLIA regulations establish quality standards for laboratory testing performed on specimens from humans, such as blood, body fluid and tissue, for the purpose of diagnosis, prevention, or treatment of disease, or assessment of health. The final CLIA regulations were published in 1992, phased in through 1994, and amended in 1993, 1995, and 2003. Visit the CLIA Documents page to search and view the Federal Register Notices and former editions of the Code of Federal Regulations (published annually in October).” What is meant by CLIA?Clinical Laboratory Improvement Amendments (CLIA)
What is CLIA and what is its purpose?What is CLIA? The Clinical Laboratory Improvement Amendments of 1988 (CLIA) is a federal program governed by the Centers for Medicare & Medicaid Services (CMS). Its purpose is to establish quality standards for clinical laboratory testing to ensure that patient test results are accurate and reliable.
Which is an independent laboratory facility that analyzes specimens sent from other healthcare facilities?Independant labs that analyze samples from other health care facilities are known as: reference labs.
What is the purpose of the Clinical Laboratory Improvement Act of 1988 quizlet?Established in 1988 to ensure quality of diagnostic testing through laboratory regulations.
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Which is a law that mandates the regulations on all facilities that perform patient testing?
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