Fda Could Issue Emergency Use Authorization For Coronavirus Vaccine In A Matter Of Weeks

BING NEWS:
  • At request of AstraZeneca, Europe withdraws marketing authorization of COVID vaccine Vaxzevria
    On Tuesday, the EMA said it had accepted a request from AZ and withdrawn (PDF) the company’s marketing authorization for its COVID-19 shot Vaxzevria. The vaccine ... the coronavirus pandemic, the U.K.
    05/8/2024 - 12:33 am | View Link
  • Labcorp's (LH) At-Home Mpox Testing Kit Gets the FDA's EUA Nod
    Laboratory Corporation of America Holdings LH, or Labcorp, recently received the FDA’s Emergency Use Authorization ... the global monkeypox vaccine and treatment market was valued at $ ...
    04/12/2024 - 3:24 am | View Link
  • FDA Approves New Rapid Coronavirus Test That Can Give Results In 45 Minutes
    But don’t rapidly jump to conclusions just yet before you hear of the details behind this emergency use authorization ... presence of the COVID-19 causing coronavirus. How rapid is rapid?
    03/22/2020 - 5:07 am | View Link
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