The US Federal Emergency Management Agency 17 August finalized an effort to mount a coordinated public-private response to the COVID-19 pandemic that has drawn industry criticism for lack of coordinat
The US Food and Drug Administration has given emergency use authorization (EUA) to the first rapid antigen test meant to diagnose whether a patient has the COVID-19 virus. While not as accurate as oth
[ Editor’s note : This article was updated on 7 April to clarify the regulatory status of the Becton Dickinson/BioMedomics serology COVID-19 test and update the status of the BioGx's rapid COVID-19
Medical supply companies won’t violate anti-trust law by collaborating to address the COVID-19 public health crisis, the US Department of Justice (DOJ) said in a 4 April letter to manufacturers. The