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CLINICAL LABORATORY IMPROVEMENT AMENDMENTS (CIA)
STATE SURVEY AGENCY CONTACTS
ALABAMA DEPARTMENT OF PUBLIC HEALTH
Division of Health Care Facilities
CIA Program
P.O. Box 303017
Montgomery, AL 361303017
(334)
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What is clinical laboratory improvement amendments?
Clinical Laboratory Improvement Amendments, also known as CLIA, are federal regulatory standards that establish quality standards for laboratory testing to ensure the accuracy, reliability, and timeliness of patient test results.
Who is required to file clinical laboratory improvement amendments?
Any laboratory that performs testing on human specimens for the purpose of diagnosis, treatment, or prevention of disease is required to comply with CLIA regulations and file the necessary amendments.
How to fill out clinical laboratory improvement amendments?
The process of filling out CLIA amendments involves completing the required forms provided by the Centers for Medicare & Medicaid Services (CMS) and submitting them electronically or by mail as instructed by the CMS.
What is the purpose of clinical laboratory improvement amendments?
The main purpose of CLIA amendments is to ensure the accuracy and reliability of laboratory testing, protect patient safety, and promote high-quality laboratory practices.
What information must be reported on clinical laboratory improvement amendments?
CLIA amendments require laboratories to report detailed information such as facility identification, personnel qualifications, quality assurance procedures, test methodologies, and proficiency testing results.
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