FDA Issues EUA for Two COVID-19 Antigen Home Tests
The U.S. Food. and Drug Administration (FDA) issued emergency use authorizations for two COVID-19 Antigen Home Tests.
Read MorePosted by Chris Wolski | Nov 22, 2022 | Covid 19 |
The U.S. Food. and Drug Administration (FDA) issued emergency use authorizations for two COVID-19 Antigen Home Tests.
Read MorePosted by Chris Wolski | Nov 21, 2022 | Covid 19 |
Researchers have shown that patients with acute COVID-19 infection have increased levels of the cytokine IL-26 in their blood.
Read MorePosted by Chris Wolski | Oct 13, 2022 | Covid 19 |
Researchers found a small group of laboratory workers whose false positive tests for the virus came not through viral RNA from plasmids.
Read MorePosted by Chris Wolski | Oct 4, 2022 | Covid 19, Flu & Respiratory Infections, Molecular Diagnostic Analyzers, POC Rapid Assays |
Cue Health has announced that it submitted an application with the FDA for EUA for its Cue Flu + COVID-19 Molecular Test.
Read MorePosted by Chris Wolski | Sep 27, 2022 | Compliance |
The FDA has updated its COVID-19 test policy to ensure continued access to tests, transitioning traditional premarket review pathways.
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