2021
DOI: 10.1002/soej.12494
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The FDA and the COVID‐19: A political economy perspective

Abstract: This article utilizes a political economy framework to examine how FDA regulations impacted the U.S. healthcare sector's ability to address COVID‐19. I specifically examine the developing COVID‐19 testing, the approval of the medication remdesivir, and COVID‐19 vaccines. By examining periods before and after the FDA issued Emergency Use Authorizations (EUAs), my analysis finds that the FDA's regulations enacted before the COVID‐19 pandemic began strongly restricted clinician and patient access to COVID‐19 test… Show more

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Cited by 12 publications
(2 citation statements)
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References 68 publications
(64 reference statements)
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“…Будучи крупным заказчиком услуг лоббистов в Конгрессе США, фармацевтические корпорации оплачивают не более 15% таких заказов (30 из 200 млн долл.). Вес вложений фармацевтов в общие расходы на лоббирование (чуть более 40 млн 12 [Яновский, Жаворонков, Черный, 2017], а также [March, 2021]. )…”
Section: защита потребителя от недоброкачественных лекарствunclassified
“…Будучи крупным заказчиком услуг лоббистов в Конгрессе США, фармацевтические корпорации оплачивают не более 15% таких заказов (30 из 200 млн долл.). Вес вложений фармацевтов в общие расходы на лоббирование (чуть более 40 млн 12 [Яновский, Жаворонков, Черный, 2017], а также [March, 2021]. )…”
Section: защита потребителя от недоброкачественных лекарствunclassified
“…In general, the study of aggregation paradoxes and public choice outcomes has received substantial treatment. Klein [25], March [26], Sobel [27], and Tabarrok [28,29], and Leeson and Thompson [30] each consider the role of the FDA in public health outcomes. Each of these studies finds government failures stemming from the FDA's decision-making criteria, where the FDA depends heavily on non-parametric efficacy tests that are subject to aggregation paradoxes.…”
Section: Introductionmentioning
confidence: 99%