Published April 26, 2021, 3:57 PM
The Food and Drug Administration (FDA) said US-based drugmaker Moderna has applied for an emergency use authorization (EUA) of its vaccine against the coronavirus disease (COVID-19) in the Philippines.
This file photo taken on November 18, 2020 shows a syringe and a bottle reading “Vaccine COVID-19” next to the Moderna biotech company logo.
(Photo by JOEL SAGET / AFP / MANILA BULLETIN)
FDA Director General Eric Domingo said the US-based drugmaker filed its emergency use authorization (EUA) application before the regulatory body on Monday, April 26.
Based on the latest data from the Department of Health (DOH), Moderna vaccine uses an mRNA technology platform, and requires two doses with 28 days apart.
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