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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 Collection COVID 19 SARS CoV 2 preprints from medRxiv SARS CoV 2 IgG and IgM/IgA antibodies were tested (COVID 19 VIRCLIA Monotest, Vircell Microbiologist, Spain; reported sensitivity 70% IgG and 89% IgM/IgA, and specificity 89% and 99% respectively). Indeterminate results were re tested (VITROS Immunodiagnostic Products Anti SARS CoV2 Total Tests, Ortho Clinical Diagnostics, USA; 100% sensitivity