Summit on human performance and dietary supplements summary report

Nutrition Today

Volumn 49, Issue 1, 2014, Pages 7-15

  Arensberg, Mary Elizabeth ^a   Costello, Rebecca ^b   Deuster, Patricia A ^b   Jones, Donnamaria ^c   Twillman, Gwen ^d  

^a ABBOTT LABORATORIES   (United States)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c Uniformed Services University of the Health Sciences   (United States)

^d American Society for Nutrition   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84894126191     PISSN: 0029666X     EISSN: 15389839     Source Type: Journal    
DOI: 10.1097/NT.0000000000000013     Document Type: Article

References (19)

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2. US Food and Drug Administration. Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006. Public Law 109-462. http://www.fda.gov/ RegulatoryInformation/Legislation/FederalFoodDrugandCosmeticActFDCAct/ Significant AmendmentstotheFDCAct/ucm148035.htm. AccessedDecember 16, 2012.
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13. Food,Drug, and Cosmetic Act. 21USC 379 aa-1, aa-2 761(a)(1,2) (2006).
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19. Department of Health and Human Services, US Food and Drug Administration. Agency Information Collection Activities; submission for Office of Management and Budget review; comment request; adverse event reporting and recordkeeping for dietary supplements as required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act. Fed Regist. Doc. no. 2012-12878.