QIAGEN Receives FDA Emergency Use Authorization for NeuMoDx Multiplex Test Expanding COVID-19 Portfolio - Business Wire
QIAGEN Receives FDA Emergency Use Authorization for NeuMoDx Multiplex Test Expanding COVID-19 Portfolio Business Wire
'Horrible' weeks ahead as India's virus catastrophe worsens - The Associated Press
'Horrible' weeks ahead as India's virus catastrophe worsens The Associated Press
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