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Business · 26/07/2007

FDA Releases Revised Draft Guidance for In Vitro Diagnostic Multivariate Index Assays

The Food and Drug Administration (FDA) has made available a revised draft guidance document addressing the definition and regulatory status of In Vitro Diagnostic Multivariate Index Assays (IVDMIAs), a class of in vitro diagnostic devices, and their premarket and postmarket requirements.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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