Radiance offers SARS-CoV-2 Real-Time reverse-transcriptase polymerase chain reaction (RT-PCR) based qualitative in vitro diagnostic test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal swab specimens, nasopharyngeal aspirate, and bronchoalveolar lavage (BAL) collected from individuals suspected of COVID-19 by their healthcare provider or for pre travel purposes. These FDA EUA-authorized multiplex real-time PCR diagnostic kits we use enable us quickly diagnose COVID-19 caused by SARS-CoV-2 infection.
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