Barely able to travel during the COVID-19 pandemic, the US Food and Drug Administration’s inspectorate used the time to plow back travel savings into bolstering other activities related to quality oversight and to develop alternatives like reviewing records remotely and relying on findings of other countries’ authorities that could increase effectiveness post-pandemic.
As FDA investigators surge back into the field, they can expect to gain additional flexibilities supported by recent experience in relying more on the findings of other countries’
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