Further, studies have shown that there is a low risk of complications. clinical trials) and the FDA must determine that the known and potential benefits outweigh the known and potential risks of the vaccine.Ī: Pfizer and Moderna vaccines have been approved for Emergency Use Authorization by the Food and Drug Administration (FDA). For an EUA to be issued for a vaccine, there must be adequate manufacturing information to ensure quality, safety, and consistency (e.g. Q: What is an Emergency Use Authorization (EUA)?Ī: According to the Food and Drug Administration (FDA), an Emergency Use Authorization is a mechanism used by the FDA to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies such as the current COVID-19 pandemic. The Pfizer and Moderna vaccines have been approved for Emergency Use Authorization by the Food and Drug Administration (FDA), a mechanism used to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies such as the current COVID-19 pandemic. Has the vaccine been officially approved for use?Ī.
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