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20:33 EDT Quidel gets emergency use authorization for Molecular COVID 19 diagnostic Quidel announced that Quidel has received Emergency Use Authorization from the FDA to market its Lyra SARS CoV 2 Assay, a real time RT PCR test intended for the qualitative detection of nucleic acid from SARS CoV 2 in nasopharyngeal or oropharyngeal swab specimens from patients suspected of Wholesale Lots and Surplus Auctions Online LiquidationAbout Liquidity Services. Liquidity Services (NASDAQLQDT) operates a network of leading e commerce marketplaces that enable buyers and sellers to transact in an efficient, automated environment offering over 500 product categories. The Company employs innovative e commerce marketplace solutions to manage, value and sell inventory and equipment for business and government sellers.Coronavirus Test Available at Randox Laboratories Randox has developed a rapid test for COVID 19 (SARS CoV 2), the new strain of coronavirus.. The game changing Viral Respiratory Tract Infection (VRI) Array is available on The Vivalytic, a molecular point of care platform brought to the market by Randox Laboratories and leading technology manufacturer Bosch Healthcare Solutions. The revolutionary VRI Array can identify SARS CoV 2 and
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Feb 06, 2020 · The test kit, called the Centers for Disease Control and Prevention (CDC) 2019 Novel Coronavirus (2019 nCov) Real Time Reverse Transcriptase (RT) PCR Diagnostic Panel (CDC 2019 nCoV Real Time RT PCR), is designed for use with an existing RT PCR testing instrument that is commonly used to test for seasonal influenza.