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CIA ANNUAL LABORATORY REGISTRY 2010 Once a year the Centers for Medicare and Medicaid Services makes available to physicians and to the public specific information (including information provided
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What is clia annual laboratory registry?
CLIA stands for Clinical Laboratory Improvement Amendments. The CLIA Annual Laboratory Registry is a mandatory reporting requirement for clinical laboratories in the United States that perform testing on human specimens for the purpose of diagnosis, prevention, or treatment of disease.
Who is required to file clia annual laboratory registry?
All clinical laboratories that perform testing on human specimens for the purpose of diagnosis, prevention, or treatment of disease are required to file the CLIA Annual Laboratory Registry.
How to fill out clia annual laboratory registry?
To fill out the CLIA Annual Laboratory Registry, laboratories must complete the necessary forms provided by the Centers for Medicare & Medicaid Services (CMS) and submit them electronically through the CMS website.
What is the purpose of clia annual laboratory registry?
The purpose of the CLIA Annual Laboratory Registry is to ensure that clinical laboratories are meeting federal regulations and quality standards for the accuracy and reliability of testing performed on human specimens.
What information must be reported on clia annual laboratory registry?
The CLIA Annual Laboratory Registry requires laboratories to report information such as the name and address of the laboratory, types of tests performed, volume of tests conducted, and personnel qualifications.
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