Clinical Laboratory Improvement Amendments (CLIA)
GPTKB entity
Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:United_States_federal_law
|
| gptkbp:administeredBy |
gptkb:Centers_for_Disease_Control_and_Prevention
gptkb:Food_and_Drug_Administration gptkb:Centers_for_Medicare_&_Medicaid_Services |
| gptkbp:alsoKnownAs |
gptkb:CLIA
|
| gptkbp:appliesTo |
laboratories performing tests on human specimens
|
| gptkbp:citation |
42 U.S.C. § 263a
|
| gptkbp:covers |
laboratories in the United States
|
| gptkbp:dateEnacted |
1988
|
| gptkbp:enactedBy |
gptkb:United_States_Congress
|
| gptkbp:establishes |
quality standards for laboratory testing
|
| gptkbp:excludes |
laboratory testing for research only
|
| https://www.w3.org/2000/01/rdf-schema#label |
Clinical Laboratory Improvement Amendments (CLIA)
|
| gptkbp:purpose |
ensure accuracy, reliability, and timeliness of test results
|
| gptkbp:regulates |
clinical laboratory testing
|
| gptkbp:requires |
laboratory certification
|
| gptkbp:bfsParent |
gptkb:Medical_laboratories
|
| gptkbp:bfsLayer |
7
|