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PRINTED: 06/12/2018 FORM APPROVEDDivision of Health Service Regulation STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION(X1) PROVIDER/SUPPLIER/CIA IDENTIFICATION NUMBER:BECKY REST HOME 1 (X4) ID PREFIX TAG.
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CLIA frequently asked questions refer to common inquiries about the Clinical Laboratory Improvement Amendments (CLIA) regulations and requirements.
Laboratories that perform testing on human specimens and are subject to CLIA regulations are required to be aware of and adhere to the frequently asked questions related to CLIA.
CLIA frequently asked questions can be addressed by referencing official CLIA guidance documents, seeking assistance from CLIA support centers, or consulting with regulatory experts.
The purpose of CLIA frequently asked questions is to provide clarity and guidance to laboratories regarding compliance with CLIA regulations, ensuring accurate and reliable testing of human specimens.
CLIA frequently asked questions may cover topics such as proficiency testing requirements, personnel qualifications, quality control measures, test categorization, and reporting of test results.
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