Jillian K Mador

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T he U.S. Food and Drug Administration (FDA) calls on advisory committees (ACs) to provide external expert advice and recommendations to “enhance FDA’s ability to protect and promote the public health and maintain the public trust” ( 1). The FDA Safety and Innovation Act (FDASIA) ( 2) was signed into law in 2012 primarily to reauthorize user-fee programs(More)
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