EVANSTON, Ill.--(BUSINESS WIRE)--Minute Molecular Diagnostics today announced that the U.S. Food and Drug Administration (FDA) granted an Emergency Use Authorization (EUA) for its rapid DASH ...
The FDA-authorized Metrix COVID/Flu molecular test detects and differentiates COVID, Flu A, and B in 20 minutes. It may be used in home and CLIA-waived settings. SANTA BARBARA, Calif., Feb. 24, 2025 ...
NEW YORK CITY (WABC) -- It could be a game changer in COVID 19 testing: A company with offices in the Tri-State area received emergency authorization from the FDA for a test that could get results ...
There have been a variety of recent updates and advances in COVID-19 testing and analysis methods. The FDA Says: Check for COVID-19 Test Expiration Date Extensions The US Food and Drug Administration ...
How long COVID develops is still largely unknown. New molecular connections are revealed in a recent study led by the Center ...
AI-enabled text-first virtual healthcare clinic Curai Health is partnering with UMass Chan Medical School to study how at-home antigen and molecular tests compare with lab PCR tests in detecting the ...
So when and how should you use them? By Dani Blum Yet again this winter, millions of Americans will wonder if a nagging cough or body aches is a sign they’re coming down with Covid or the flu. This ...
SANTA BARBARA, Calif., Feb. 24, 2025 /PRNewswire/ — Aptitude Medical Systems, Inc. (Aptitude) today announced it has received Emergency Use Authorization (EUA) from the U.S. Food and Drug ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results