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The shortage is due to an issue with manufacturing an lively pharmaceutical ingredient used within the drug. It is important to note that there are other options that can be used by patients. FDA actions on updates to the CURE ID crowd-sourcing app, an EUA for the first COVID-19 diagnostic test using next-generation gene sequencing, and more in FDA's ongoing response to the COVID-19 pandemic. FDA's work to advance remedies for uncommon illnesses and helping ensure continuity of take care of folks with uncommon illnesses remain prime priorities during COVID-19. Food and Drug Administration revoked the emergency use authorization of the Chembio Diagnostic System, Inc. DPP COVID-19 IgM/IgG System, a SARS-CoV-2 antibody check, as a end result of efficiency issues with the accuracy of the test. FDA actions on a web useful resource itemizing EUAs, the CURE ID app, and extra in its ongoing response to the COVID-19 pandemic. 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Help youngsters find positive methods to express disturbing emotions corresponding to fear and unhappiness. FDA actions on diagnostic exams, together with authorizations, and more in its ongoing response to the COVID-19 pandemic. FDA actions on revocation of EUAs, updates on the Coronavirus Treatment Acceleration Program, warning letters and more in its ongoing response to the COVID-19 pandemic. The FDA issued an emergency use authorization to Yale School of Public Health for its SalivaDirect COVID-19 diagnostic test, which uses a brand new method of processing saliva samples. FDA's actions on a warning letter, an permitted abbreviated new drug application, and an updated steerage in its ongoing response to the COVID-19 pandemic. FDA's actions on a re-issued EUA, an update to the Device Discontinuance List and new health education materials in its ongoing response to the COVID-19 pandemic. 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시간: 3월 25, 2022 Comments