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Zdrowie i gospodarka · 21/07/2000

FDA to Host Public Workshop on CLIA Waiver Criteria for Medical Devices

The U.S. Food and Drug Administration (FDA) will host a public workshop to discuss and clarify the criteria for medical devices to obtain a Clinical Laboratory Improvement Amendments (CLIA) waiver, a process that allows certain devices to be used in clinical settings without the need for CLIA certification.

Source: Federal Register — Food and Drug AdministrationOpen original release →