Nirmidas Biotech received FDA Emergency Use Authorization for its COVID-19 rapid antibody fingerstick test
On Jan. 25, 2021, Nirmidas Biotech announced its second FDA Emergency Use Authorization (EUA) for their COVID-19 rapid antibody IgG/IgM test, now available for point-of-care (POC) settings. The MidaSpotル COVID-19 Antibody Combo Detection Kit uses a fingerstick serology test for detecting antibodies against the RBD antigen on the surface of the SARS-CoV-2 virus.
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Source: Businesswire
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