27 Oct Over the last few years due to the COVID-19 pandemic we have seen rapid development of diagnostics, vaccines and therapeutics under Emergency Use Authorization (EUA)
Over the last few years due to the COVID-19 pandemic we have seen rapid development of diagnostics, vaccines and therapeutics under Emergency Use Authorization (EUA). FOr information on this process see the FDA website: Emergency Use Authorization. What is the EUA process? How does it affect development plans in the short-term? What about in the long-term? Discuss examples of products developed under the EUA process for the COVID-19 pandemic. Discuss how product development plans and timelines were for specific products were affected. What have we learned from all of this?
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