The CLINITEST Rapid COVID-19 Antigen Self-Test has received FDA EUA for unsupervised self-testing for the SARS-CoV-2 virus by individuals age 14 and older (or adult-collected samples from individuals ...

In a study involving nearly 1,000 patients seen at the Baltimore Convention Center Field Hospital (BCCFH) during a five-month period in 2022 - researchers at Johns Hopkins Medicine, the University of ...

In a study involving nearly 1,000 patients seen at a Baltimore field hospital during a five-month period in 2022, researchers at Johns Hopkins Medicine, the University of Maryland School of Medicine, ...

The Food and Drug Administration is making it easier for people to simultaneously test themselves for COVID-19 and the flu at home. The agency this week authorized the Healgen Scientific's Rapid Check ...

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, ...

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The FDA has cleared the Healgen Rapid Check COVID-19/Flu A&B Antigen Test for over-the-counter use. The Food and Drug Administration (FDA) has cleared the Healgen Rapid Check COVID-19/Flu A&B Antigen ...

The question quickly arose whether existing rapid antigen tests could detect newly emerging variants. Using clinical samples obtained from diagnostic labs throughout the U.S. from 2020 to 2023, the ...

The potential for IgM cross-reactivity with rheumatoid factor–positive serum samples was observed in blood tests used to detect IgM SARS-CoV-2 by means of gold immunochromatographic and enzyme-linked ...

Please provide your email address to receive an email when new articles are posted on . Of plasma samples taken after COVID-19 infection, 7.5% to 12.6% contained detectable viral antigens. Researchers ...