1999
DOI: 10.3949/ccjm.66.4.213
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Management of perimenopause: Focus on alternative therapies

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“…Manufacturers would not be required to provide information to FDA before marketing a product. There would be no premarketing review or approval of supplement ingredients [54]. Once a dietary supplement was marketed, the FDA would bear the burden for demonstrating that the product was unsafe prior to taking any action to restrict its use [55,56].…”
Section: The 1994 Dietary Supplement Health and Education Act (Dshea)mentioning
confidence: 99%
“…Manufacturers would not be required to provide information to FDA before marketing a product. There would be no premarketing review or approval of supplement ingredients [54]. Once a dietary supplement was marketed, the FDA would bear the burden for demonstrating that the product was unsafe prior to taking any action to restrict its use [55,56].…”
Section: The 1994 Dietary Supplement Health and Education Act (Dshea)mentioning
confidence: 99%