FDA updates EUA for COVID-19 convalescent plasma
![FDA product update](/sites/default/files/styles/900x400/public/2018-04/FDA%20product%20update.jpg?itok=TkhlK6rs)
The Food and Drug Administration last week revised and reissued its emergency use authorization for COVID-19 convalescent plasma to treat hospitalized patients with COVID-19.
The changes include updates based on additional clinical trials; clarify the authorization’s limit to high-titer convalescent plasma for hospitalized patients early in the disease and those with impaired humoral immunity; and add to the tests acceptable for qualifying high-titer COVID-19 convalescent plasma.
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