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 SD Biosensor Standard Q COVID-19 Ag Test and Acon Biotech Flowflex SARS-CoV-2 Antigen Rapid Test were previously listed under WHO's emergency use listing.
For the first time, the World Health Organization (WHO) has prequalified two rapid antigen tests for detecting COVID-19, the ...
WHO prequalifies the first two rapid antigen detection tests for Covid-19: Geneva Saturday, December 27, 2025, 11:00 Hrs [IST] The World Health Organization (WHO) announced the pr ...
More than two years after the World Health Organization (WHO) declared an end to the emergency phase of the Covid-19 pandemic ...
A recent study posted on the medRxiv* preprint server has assessed the sensitivity of antigen-based rapid diagnostic tests (Ag-RDTs). Study: Comparison of the analytical and clinical sensitivity of ...
In a recent article published in the journal ACS Sensors, a group of researchers developed a rapid, non-invasive, point-of-care platform for the direct detection of severe acute respiratory syndrome ...
New research suggests it is safe to operate on patients 2 weeks after a positive COVID test, rather than the current recommendation of 7 weeks, so long as they have recovered. Surgical decision making ...
The World Health Organization (WHO) has reached a pivotal moment in the fight against COVID-19 by prequalifying the first two rapid antigen diagnostic tests for SARS-CoV-2. This groundbreaking ...
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