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Zdrowie i gospodarka · 07/09/2005

FDA Releases Draft Guidance for Clinical Laboratory Waiver Applications

The Food and Drug Administration (FDA) has released a draft guidance recommending an approach for determining whether a laboratory test can be performed by laboratories with a certificate of waiver under the Clinical Laboratory Improvement Amendments of 1988 (CLIA).

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