(HealthDay)—The first rapid test to detect the HIV-1 antigen, as well as blood antibodies for the HIV-1 and HIV-2 strains, has been approved by the U.S. Food and Drug Administration.
Aug 9, 2013
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U.S. health officials have authorized two more over-the-counter COVID-19 tests that can be used at home to get rapid results.
Apr 1, 2021
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(HealthDay) -- The first DNA test to help doctors treat a common viral infection in people who have had a solid organ transplant has been approved by the U.S. Food and Drug Administration.
Jul 5, 2012
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What's the status of the COVID-19 vaccine mandate in the U.S.?
Dec 2, 2021
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A new type of COVID test is set to be available from November for Australians to use at home.
Oct 6, 2022
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President Joe Biden's administration on Tuesday announced it would develop a new policy requiring cigarette producers to reduce nicotine to non-addictive levels—a move that would deal a powerful blow to the tobacco industry.
Jun 21, 2022
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(HealthDay)—The Trump administration has blocked the U.S. Food and Drug Administration from regulating a wide swath of laboratory tests, including ones for the coronavirus.
Aug 21, 2020
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If there's anyone in the United States who can see the future of medicine, it's Dr. Janet Woodcock.
Sep 6, 2019
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U.S. regulators have approved a new drug that harnesses the immune system to treat advanced bladder cancer.
May 1, 2017
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Two studies carried out by US researchers and published by The BMJ today raise questions about whether most new drugs are any more effective than existing products or whether they have been adequately assessed before approval.
Sep 23, 2015
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