FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection The US Food and Drug Administration (FDA) on Friday granted the first emergency use authorization (EUA) ...
Our side-by-side test comparison of over 75 patient samples demonstrated that the use of saliva to extract viral RNA was in fact a robust source for COVID-19 detection and equal in performance to the ...
The authors and others have found that saliva samples tested after two or more days after collection are easier to extract and process. Thus, “A key takeaway from this work is the importance of ...
This morning BioIQ, a health-testing and biometric-screening technology company, released its at-home COVID-19, Flu A/Flu B, and 21 Test Respiratory Panel saliva test. The company partnered with P23 ...
A team of researchers at the University of Washington have designed a novel (and unique!) way to collect saliva samples for testing, particularly from children: a special type of lollipop. This ...
SALT LAKE CITY--(BUSINESS WIRE)--Spectrum Solutions, LLC today announced its SDNA-1000 saliva collection device has secured U.S. Food and Drug Administration (FDA) EUA authorization. Spectrum’s ...
The gold standard for the diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently based on detection using quantitative reverse-transcription polymerase chain reaction ...
Dublin, April 29, 2026 (GLOBE NEWSWIRE)-- The "Saliva Collection and Diagnostics Market Report by Site of Collection, Application, Countries and Companies Analysis 2026-2034" has been added to ...
Philadelphia, December 10, 2020 - Researchers at Memorial Sloan Kettering Cancer Center (MSK) have found that SARS-CoV-2 genetic material can be reliably detected in self-collected saliva samples at a ...
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