Mar
2
FDA Grants Emergency Use Authorization for Single-Dose Vaccine
The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) to the Janssen Pharmaceuticals Companies, a subsidiary of Johnson & Johnson, for its single-shot COVID-19 vaccine. This marks the third vaccine to be awarded an emergency use authorization by the FDA. “This week marked a devastating milestone of 500,000 deaths from … Read more