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9:24
INTERVIEW: UCSF on Moderna's COVID-19 booster emergency use by FDA
INTERVIEW: An FDA panel voted unanimously today to recommend emergency use authorization for a booster dose of Moderna's COVID-19 vaccine. UCSF...
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Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is too easy and, as a result, too many drugs are approved that are later found to be unsafe. On the other hand, a number of industry lobbyists have pushed for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is s
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