Washington, US | XINHUA | The U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) on Sunday for investigational convalescent plasma for the treatment of COVID-19 in hospitalized patients. It is part of the agency’s ongoing efforts to fight COVID-19. Based on scientific evidence available, the FDA …
Read More »EU funds for equipment to extract plasma from COVID-19 survivors
Brussels, Belgium | XINHUA | The European Union (EU) has made available up to 40 million euros (47.1 million U.S. dollars) to purchase specialized equipment to increase the collection of plasma from COVID-19 survivors for the treatment of people who contract the disease, the European Commission said Friday in a …
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