Zdrowie i gospodarka · 14/08/2015

FDA Releases Draft Guidance on In Vitro Diagnostic Devices for Human Papillomavirus Detection

The Food and Drug Administration (FDA) has released a draft guidance document outlining the performance characteristics of in vitro diagnostic devices for detecting or differentiating human papillomaviruses (HPVs). The document is intended to aid in the development of IVDs for HPV detection and is not yet finalized or effective.