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Abbott Receives EUA for COVID-19 IgM Antibody Blood Test americanpharmaceuticalreview
October 16, 2020Abbott announced the U.S. Food and Drug Administration (FDA) issued Emergency Use Authorization (EUA) for the company's AdviseDx SARS-CoV-2 IgM (Immunoglobulin M) lab-based serology test for use on the ARCHITECT? and Alinity? platforms.
Pharma Sources Insight January 2025
