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U.S. FDA issues emergency use authorisation for 10-minute rapid home-test kit for COVID-19

March 2, 2021 10:48 GMT
Determining whether one is infected with COVID-19 could now become much easier. The U.S. Food and Drug Administration (FDA) issued an emergency use authorisation on a rapid home-test kit that will yield the result in a matter of 10 minutes.
One can avail of these tests through a prescription and those who can use it are individuals who are 14 years old and older. Although those who are eight years old and above can also use the test, the presence of an adult is a requirement to collect the nasal swab sample among younger individuals.
New name for long COVID: Fauci refers to long-term coronavirus effects as PASC ....

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4th at-home COVID-19 test gets emergency use authorization from FDA

4th at-home COVID-19 test gets emergency use authorization from FDA
fox5atlanta.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from fox5atlanta.com Daily Mail and Mail on Sunday newspapers.

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4th at-home COVID-19 test gets emergency use authorization from FDA

4th at-home COVID-19 test gets emergency use authorization from FDA
fox13news.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from fox13news.com Daily Mail and Mail on Sunday newspapers.

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FDA grants emergency use authorization for QuickVue At-Home COVID-19 Test

Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the Quidel QuickVue At-Home COVID-19 Test, another antigen test where certain individuals can rapidly collect and test their sample at home, without needing to send a sample to a laboratory for analysis. ....

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NIH to evaluate COVID-19 at-home testing system

HIN
A research team funded by the National Institutes of Health has launched a study to assess performance and usability of a smartphone app paired with the Quidel QuickVue At-Home COVID-19 Test, which just received an Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration for use with a prescription. The home test was supported by NIH through the Rapid Acceleration of Diagnostics (RADx) initiative, which has spurred the development and commercial availability of millions of COVID-19 tests over the past year.
More than 200 participants have already enrolled in the study that involves daily testing for a two-week period. An app called MyDataHelps, developed by CareEvolution, LLC provides step-by-step instructions for taking the test and important tools such as timers to ensure that the steps of the test are performed at the correct time intervals. Although users can interpret the test result on their own, the app also provides an independent confirmati ....

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