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Zdrowie i gospodarka · 09/11/2012

FDA Releases Draft Guidance for Highly Multiplexed Microbiological/Medical Countermeasure In Vitro Diagnostic Devices

The FDA is releasing a draft guidance document outlining recommendations for the development and testing of in vitro diagnostic devices that can detect multiple pathogens from a single human specimen, with the goal of establishing their analytical and clinical performance.

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