FDA grants emergency use authorization for QuickVue At-Home

Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the Quidel QuickVue At-Home COVID-19 Test, another antigen test where certain individuals can rapidly collect and test their sample at home, without needing to send a sample to a laboratory for analysis.

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Jeff Shuren , Emily Henderson , Radiological Health , Clinical Laboratory Improvement Amendments , Drug Administration , Quidel Quickvue At Home , Quickvue At Home , Antigen , Laboratory , எமிலி ஹென்டர்சன் , கதிரியக்கவியல் ஆரோக்கியம் , மருத்துவ ஆய்வகம் முன்னேற்றம் திருத்தங்கள் , ஆய்வகம் ,