ARTICLE
11 January 2016

FDA Creates New Office For Dietary Supplements

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Jones Day

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The creation of the new office is a reflection of FDA's efforts to step up regulation of the supplement industry in response to public health concerns.
United States Food, Drugs, Healthcare, Life Sciences

FDA has announced the creation of the new Office of Dietary Supplement Programs ("ODSP"), a program that has existed for 20 years as a division of FDA's Office of Nutrition Labeling and Dietary Supplements. Creation of the ODSP underscores the growth of the dietary supplement industry, from about $6 billion to more than $35 billion in annual sales, over those same 20 years. According to the Agency, "[e]levating the program's position will raise the profile of dietary supplements within the agency, and will enhance the effectiveness of dietary supplement regulation by allowing ODSP to better compete for government resources and capabilities to regulate this rapidly expanding industry."

The creation of the new office is a reflection of FDA's efforts to step up regulation of the supplement industry in response to public health concerns. ODSP will use existing resources to monitor dietary supplements on the marketplace. ODSP's former parent office will continue its other activities under the shortened name, the Office of Nutrition and Food Labeling, and the leadership of Doug Balentine, who recently joined FDA. Balentine will oversee the development of policy and regulation for nutrition labeling and food standards, infant formula, and medical foods.

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