QuickVue® was also the first flu test cleared by the FDA for use in CLIA-Waived point-of-care facilities like doctors’ offices, urgent care clinics and pharmacies. Today, QuickVue® is a market leading ...
SAN DIEGO, Sept. 22, 2025 /PRNewswire/ -- Building on its leadership in point-of-care diagnostic testing, QuidelOrtho Corporation (Nasdaq: QDEL) ("QuidelOrtho"), a leading global provider of ...
SAN DIEGO--(BUSINESS WIRE)-- Quidel Corporation (NASDAQ: QDEL) (“Quidel”), a leading provider of rapid diagnostic testing solutions, cellular-based virology assays and molecular diagnostic systems, ...
A new at-home COVID test has received emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA). Below is what you need to know about the at-home test. How can I get a Quidel ...
SAN DIEGO (KGTV) -- A San Diego company just got emergency authorization from the Food and Drug Administration to sell a self-test for COVID-19 that returns results in 10 minutes, entirely from home.
SAN DIEGO--(BUSINESS WIRE)-- Quidel Corporation (NASDAQ: QDEL) (“Quidel”), a leading provider of rapid diagnostic testing solutions, cellular-based virology assays and molecular diagnostic systems, ...
Quidel, a developer of rapid diagnostic testing solutions, has received an Emergency Use Authorization from the U.S. Food and Drug Administration, allowing the company to market its new QuickVue ...
A San Diego-based diagnostic health care manufacturer was granted emergency approval Monday for its at-home COVID-19 test by the U.S. Food and Drug Administration and plans to ramp up production in ...
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 ...
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