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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. The food and drug administration (fda), centers for. Pages in category clinical laboratory improvement amendments the following 3 pages are in this category, out of 3 total
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This list may not reflect recent changes. [34] three federal agencies partner together to cover the responsibilities put forward in the regulations Clia stands for clinical laboratory improvement amendments, and facilities with these certificates meet certain requirements for quality laboratory testing.
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 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. The clinical laboratory improvement amendments (clia) regulate any laboratory testing and require laboratories to obtain certificates to do any testing on human specimens for health assessment or to diagnose, prevent, or treat disease
