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January 2021 From: Chianti M. Lu, MD / Jakarta CIA Lab Director Dear Client, Jakarta CIA Laboratory Services provides FDA EUA approved COVID-19 test that detects SARS CoV2 in clinical specimens. This
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LU MD Diacarta CLIA is a reference to a specific document or requirement related to the Clinical Laboratory Improvement Amendments (CLIA), which governs laboratory testing in the United States.
Facilities that perform laboratory testing and are subject to CLIA regulations are required to file LU MD Diacarta CLIA.
Filling out LU MD Diacarta CLIA typically involves providing accurate facility information, test types, and compliance details, often guided by specific instructions provided by CLIA.
The purpose of LU MD Diacarta CLIA is to ensure that laboratory testing meets federal standards for quality and accuracy, thereby protecting public health.
Information reported on LU MD Diacarta CLIA includes laboratory details, types of tests conducted, and compliance with safety and quality standards.
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