FDA in the Time of COVID-19

Abstract

Over the past century, Congress has made the Food & Drug Administration (FDA) responsible for regulating the safety and efficacy of drugs and devices being deployed in the fight against the COVID-19 pandemic. The FDA’s regulatory infrastructure was built for public health threats and to combat manufacturers' misinformation about treatments. This article spotlights the ways in which FDA has been adapting to a new challenge during the COVID-19 pandemic: combating misinformation emanating from within the executive branch.

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Keywords: FDA, COVID-19, coronavirus, misinformation, public health, executive, administrative law, regulation, agency, publicity, pharmaceutical