Testing And Clinical Laboratory Improvement Amendments Of
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Center for Clinical Standards and Quality/Survey ...
www.cms.govSUBJECT: Clinical Laboratory Improvement Amendments of 1988 (CLIA) Laboratories ... number, type, frequency of testing, and criteria for acceptable result(s) of the quality control(s), and must be approved by the laboratory director. D. Specimen Type
Clinical Laboratory Improvement Amendments (CLIA)
www.cms.govNOTE: Congress passed the Clinical Laboratory Improvement Amendments (CLIA) in 1988 establishing authority to promulgate standards for certain laboratory testing to ensure the accuracy, reliability and timeliness of test results regardless of where or by whom the test was performed. The CLIA requirements are based on the complexity of the test
Retention Laboratory Records and Materials
elss.cap.orgrequirements specified in the Clinical Laboratory Improvement Amendments of 1988 (CLIA 88). It may be appropriate for laboratories to retain records and/or materials for a longer period of time when required for patient care, education, quality improvement, medical/legal, or other needs, or if required by institutional policy.
Laboratory, Pathology Clinical - Nevada
www.medicaid.nv.govFeb 02, 2022 · Clinical laboratories must have current and appropriate Clinical Laboratory Improvement Amendments (CLIA) certification for any laboratory test performed, except CLIA waived tests. State Policy The Medicaid Services Manual (MSM) is on the Division of Health Care Financing and Policy (DHCFP) website at