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PRINTED: 03/23/2022 FORM APPROVEDDEPARTMENT OF HEALTH AND HUMAN SERVICES CENTERS FOR MEDICARE & MEDICAID SERVICES STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION(X1) PROVIDER/SUPPLIER/CIA IDENTIFICATION
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01
Obtain the necessary CLIA documents from the CDC website or local health department.
02
Carefully read the instructions for each section of the CLIA documents.
03
Fill out all required information accurately and completely, including your laboratory's CLIA number and certificate type.
04
Include any necessary supporting documentation, such as proof of accreditation or certifications.
05
Double check all information for accuracy before submitting the completed documents to the CDC.

Who needs clia documents - cdc?

01
Any laboratory that performs clinical testing on human specimens is required to have CLIA documents from the CDC.
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CLIA documents - CDC stand for Clinical Laboratory Improvement Amendments documents issued by the Centers for Disease Control and Prevention.
Clinical laboratories in the United States are required to file CLIA documents with the CDC.
CLIA documents can be filled out electronically through the CDC's online portal or by submitting physical forms via mail.
The purpose of CLIA documents is to ensure that clinical laboratories meet certain quality standards in order to provide accurate and reliable test results.
CLIA documents must include information about the laboratory's personnel qualifications, testing procedures, quality control measures, and proficiency testing results.
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