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The Clinical Laboratory Improvement Amendments (CLIA) of 1988 are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, except clinical trials and basic research.
Following California, several states including Massachusetts and Missouri attempted to introduce either licensure or training/educational requirements, but the bills died. [ 1 ] [ 2 ] [ 3 ] Phlebotomy licensure advocates claim that the licensure would enhance the quality of personnel, while the laboratory industry opposes phlebotomy licensure ...
English: A brochure outlining the changes for the 2003 Clinical Laboratory Improvement Amendments (CLIA) regulations. Date: 2003: Source:
In some cases, Medicare may require testing within a Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory. Additionally, further criteria may apply to each type of genetic test ...
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The Individualized Quality Control Plan (IQCP) is a quality management system under the US Clinical Laboratory Improvement Amendments (CLIA) federal regulatory standards. It is designed to enable regulated medical laboratories to manage the frequency of their quality control. [1] [2]
Laboratories first began receiving CAP accreditation in 1964, [8] and the organization was later given authority to accredit medical laboratories as a result of the Clinical Laboratory Improvement Amendments of 1988. [9] The CAP publishes checklists containing requirements pertaining to the performance of laboratory tests.
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