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What is ILIA and CLIA?

ILIA refers to the International Laboratory Improvement Act, and CLIA stands for the Clinical Laboratory Improvement Amendments, which are U.S. federal legislation that regulates laboratory testing.

Who is required to file ILIA and CLIA?

All clinical laboratories that perform tests on human specimens for health assessment or to diagnose, prevent, or treat disease are required to file under CLIA.

How to fill out ILIA and CLIA?

ILIA and CLIA forms are filled out by providing laboratory information, including ownership, type of testing performed, and compliance with health and safety standards, through the designated federal or state health agency portal.

What is the purpose of ILIA and CLIA?

The purpose of ILIA and CLIA is to ensure quality laboratory testing and enhance laboratory standards to protect public health.

What information must be reported on ILIA and CLIA?

Laboratories must report their ownership details, types of tests performed, compliance levels with federal regulations, and any accreditation information.