RAPS

FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection

The US Food and Drug Administration (FDA) on Friday granted the first emergency use authorization (EUA) allowing for at-home saliva sample collection for a coronavirus disease (COVID-19) diagnostic ...
RAPS

FDA authorizes first COVID-19 test for at-home sample collection

The US Food and Drug Administration (FDA) on Tuesday granted an emergency use authorization (EUA) to LabCorp allowing it to test self-collected nasal swab samples from patients for coronavirus disease ...

The best at-home COVID-19 test for 2026

With so many at-home Covid rapid testing options on the market, figuring out which COVID test is right for you can be hard, ...
Business Wire

Rheonix COVID-19™ MDx Assay Receives Expanded FDA Emergency Use Authorization to Include Saliva Home Collection Kit

ITHACA, N.Y.--(BUSINESS WIRE)--Rheonix Inc. announced today that the United States Food and Drug Administration (FDA) has issued an expanded Emergency Use Authorization (EUA) for the Rheonix COVID-19™ ...