FDA Draft Guidance Fails To Deliver On AER Label Addresses – CSPI
The Center for Science in the Public Interest urges FDA to require complete addresses on OTC and supplement product labels for compliance with the adverse event reporting law that goes into effect Dec. 22
Learn what's happening at the US FDA. On the go.
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Revised recommendation is based on most recent data on circulating strains in US, where KP.3 is now dominant. Novavax sticks with plans targeting the JN.1 ‘parent strain.’
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Pink Sheet reporter and editors discuss the US FDA’s changes to the COVID-19 vaccine indication and its revocation of the vaccine emergency use authorizations, as well as new vaccine coverage and reimbursement questions.
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