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Abbott Receives Emergency Use Authorization For COVID-19 Test

 
• By Catherine Longworth

Abbott has become the next major diagnostics company to receive an Emergency Use Authorization from the US FDA for a COVID-19 test.  

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The US Food and Drug Administration has issued Emergency Use Authorization (EUA) to Abbott Laboratories Inc. for a COVID-19 test, the company announced 18 March.

Abbott said it will ship 150,000 Abbott RealTime SARS-CoV-2 EUA tests to existing customers in the US and ramp up...

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