The U.S. Food and Drug Administration granted Emergency Use Authorization to a diagnostic test for at-home, self-collection of patient samples for the detection of SARS-CoV-2 and influenza A/B.
The U.S. Food and Drug Administration granted Emergency Use Authorization to a diagnostic test for at-home, self-collection of patient samples for the detection of SARS-CoV-2 and influenza A/B.
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