NEWS MAKER

@NEWS_MAKER ↗

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Last Checked Oct. 23, 2021

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Sat Jul 24 18:09:20 +0000 2021

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NEWS MAKER @NEWS_MAKER

in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives. — PolitiTweet.org

Posted July 24, 2021 Hibernated

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NEWS MAKER @NEWS_MAKER

After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for EMERGENCY USE AUTHORIZATION (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced — PolitiTweet.org

Posted July 24, 2021 Hibernated

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NEWS MAKER @NEWS_MAKER

In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and — PolitiTweet.org

Posted July 24, 2021 Hibernated