The Centers for Medicare & Medicaid Services (CMS) regulates all laboratory testing (except research) performed on humans in the U.S. through the Clinical Laboratory Improvement Amendments (CLIA) …

CLIA unites the global cruise industry by providing a strong collective voice for cruise lines, valuable connections and insights for Executive Partners, and training, resources, and support for the travel …

Sep 11, 2024 · The Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations include federal standards applicable to all U.S. facilities or sites that test human specimens for health …

In 2019 CLIA proposed a new set of quality requirements for proficiency testing. They were updated July 11, 2022. They became official law on July 11,2024. They were fully implemented by proficiency …

Nov 30, 2025 · What is CLIA? The Clinical Laboratory Improvement Amendments (CLIA) of 1988 applies to facilities or sites that test human specimens for health assessment or to diagnose, prevent, …

CLIA certification is required for facilities that test clinical specimens for the purpose of diagnosis, treatment, or prevention of disease.

Apr 23, 2024 · The Clinical Laboratory Improvement Amendments (CLIA) is the federal program that establishes quality laboratory standards to protect patient safety and improve healthcare for …

The Clinical Laboratory Improvement Amendments (CLIA) is a set of regulatory standards that apply to all clinical laboratory tests performed on humans. The CLIA program is operated by the Centers for …

The Clinical Laboratory Improvement Amendments (CLIA) of 1988 are United States federal regulatory standards that apply to all clinical laboratory testing performed on humans in the United States, …

Within FDA, CLIA categorization is conducted by the Center for Devices and Radiological Health (CDRH). The FDA tracks CLIA categorizations through CLIA Record (CR) submissions.