EVANSTON, IL — Is it possible you were infected with a mild form of COVID-19 and didn’t know it? How robust is your body’s immune response to the vaccine, and how will we know whether we’ve reached ...
CHICAGO (NewsNation Now) — The U.S. Food and Drug Administration (FDA) issued an emergency use approval for Abbott’s latest lab-based COVID-19 IgM antibody test, the company announced Monday. Abbott ...
As the world continues to navigate the aftermath and lingering presence of COVID-19, one question remains as relevant as ever: Which COVID-19 test is right for me—diagnostic or antibody? Whether ...
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, ...
Editor's note: Find the latest COVID-19 news and guidance in Medscape's Coronavirus Resource Center. The U.S. Food and Drug Administration has granted Cellex an emergency use authorization to market a ...
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