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Zdrowie i gospodarka · 15/09/2017

FDA Announces Guidance for Human Papillomavirus Diagnostic Devices

The Food and Drug Administration (FDA) has released a new guidance document outlining the performance characteristics of in vitro diagnostic devices for detecting or differentiating human papillomaviruses (HPVs), replacing a previous version from 2011.

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