Plenty of things have changed in the two years since the start of the COVID-19 pandemic. For example, think about how many people now know the difference between a rapid antigen test and a nucleic ...
Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the Cue COVID-19 Test for Home and Over The Counter (OTC) Use. The product is a molecular nucleic acid ...
The currently available tests for detecting antigen load in patients suspected of being infected with the severe acute respiratory syndrome coronavirus (SARS-CoV-2) include the rapid antigen and ...
A rapid, highly accurate test has been developed for diagnosing hepatitis C virus (HCV), according to a study published online Dec. 10 in the Journal of Infectious Diseases. A comprehensive eight-year ...
Cue Health Inc. became the first company to offer COVID-19 molecular testing for home use without a prescription following U.S. FDA emergency use authorization on March 5, 2021. The San Diego-based ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results