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Top takeaways from FDA regulatory session at SupplySide East

The U.S. Food & Drug Administration's good manufacturing practice (GMP) inspections of dietary supplement facilities is back up to 500 per year, a return to pre-COVID levels, but those levels are still inadequate, says Dr. Cara Welch, FDA’s director of the Office of Dietary Supplement Programs (ODSP). ....

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ODSP's Welch: NDIN 'guidances are not enforceable'

FDA’s director of the Office of Dietary Supplement Programs (ODSP), Cara Welch, PhD, stopped by SupplySide East to present an overview of the agency’s FY23 activities related to dietary supplements and FY24 plans as well as an update on the pending Human Foods Program reorganization. She sat down with NutraIngredients-USA to discuss these topics and more. ....

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UNPA's Israelsen calls for resolution of NDI issue

Loren Israelsen, president of the United Natural Products Alliance (UNPA) and one of the key architects of the Dietary Supplement Health and Education Act (DSHEA), is urging the Food and Drug Administration (FDA) to “move along as quickly as they can” to finalize any outstanding sections of the New Dietary Ingredient guidance. ....

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