The Clinical Laboratory Improvement Amendments (CLIA) program is a federal regulatory program that establishes quality standards for laboratory testing. Laboratories that perform testing on human specimens for the diagnosis, prevention, or treatment of disease are required to be CLIA-certified. However, there are some laboratories that may qualify for a CLIA waiver. A CLIA waiver is…
The Clinical Laboratory Improvement Amendments (CLIA) program establishes quality standards for all laboratory testing performed on human specimens in the United States. Laboratories must be certified under CLIA to perform testing. The CLIA certification process can be complex and time-consuming, but it is essential for laboratories that wish to provide accurate and reliable testing services….
The Clinical Laboratory Improvement Amendments (CLIA) waiver program is a federal program that allows certain laboratories to perform certain tests without having to meet all of the CLIA requirements. This program is designed to make it easier for small laboratories to provide testing services to their patients. To apply for a CLIA waiver, a laboratory…
