CAP TODAY Pathology/Laboratory Medicine/Laboratory Management
April 1, 2021—DiaSorin received emergency use authorization from the FDA for its Liaison SARS-CoV-2 Ag.
The test uses chemiluminescence immunoassay technology to determine the presence of SARS-CoV-2 nucleocapsid protein antigen in anterior nasal dry swabs and nasopharyngeal swabs, eluted in universal transport medium, and is used to assist in the diagnosis of acute COVID-19 infection through qualitative detection of the virus.
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