In a recent study posted to the medRxiv* server, researchers evaluated a rapid antigen test (RAT) that used saliva specimens to detect the presence of severe acute respiratory syndrome coronavirus 2 ...

Saliva-based method enables simpler and quicker collection of samples Entirely UK researched, developed and manufactured lateral flow COVID-19 antigen test Designed to support COVID-19 testing in ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. (NEXSTAR) – The U.S. Food and Drug ...

STATEN ISLAND, N.Y. -- The U.S. Food and Drug Administration (FDA) is warning people to stop using the LuSys Laboratories COVID-19 Antigen Test (Nasal/Saliva) and the LuSys Laboratories COVID-19 ...

The U.S. Food and Drug Administration is warning people to stop using two COVID-19 tests produced by LuSys Laboratories, citing a high risk of false results when using the tests. The LuSys ...

The FDA has issued emergency authorizations to 12 antibody tests for the virus. As federal officials gradually begin reopening the country, expanded testing is central to the conversation. Until now, ...

SALT LAKE CITY--(BUSINESS WIRE)--Spectrum Solutions, LLC today announced the U.S. Food and Drug Administration (FDA) has extended its Emergency Use Authorization for the SDNA-1000 Saliva Collection ...

We’re entering a phase in the COVID-19 pandemic where transmission is going to go through the roof because of the Delta variant. But as vaccinations ramp up around the world, the main cost to society ...

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The authors do not work for, consult, own shares in or receive funding from any company or organization that would benefit from this article, and have disclosed no relevant affiliations beyond their ...