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| Name | Dietary Supplement Practicum (2 of 21): What the U.S. Food & Drug Administration (FDA) Does |
| Video Uploader | Video From National Institutes of Health (NIH) |
| Upload Date | This Video Uploaded At 01-11-2017 12:29:01 |
| Video Discription | (Bethesda, MD) Sibyl Swift, Ph.D., special assistant in the U.S. Food and Drug Administration’s (FDA) Office of Dietary Supplement Programs, talks about the FDA’s dietary supplement-related responsibilities and how the FDA’s regulation of dietary supplement products differs from those covering conventional foods and medicine. Dr. Swift explains the FDA’s role in regulating supplements versus the manufacturer’s responsibility for marketing them, as well as FDA’s post-marketing responsibilities for supplements, including safety monitoring and the provision of product information. She provides examples of the types of regulatory actions FDA has taken against potentially harmful and/or mislabeled supplements. This presentation is part of the 2017 Mary Frances Picciano Dietary Supplement Research Practicum sponsored by the NIH Office of Dietary Supplements (ODS). This 2.5-day annual event for faculty, students, and health practitioners provides a thorough overview of issues, concepts, unknowns, and controversies about dietary supplements and supplement ingredients. It also emphasizes the importance of scientific investigations to evaluate the efficacy, safety, and value of these products for health promotion and disease prevention as well as how to carry out this type of research. For more information: https://ods.od.nih.gov/Research/dsrp.aspx |
| Category | Science & Technology |
| Tags | Sibyl Swift | Food and Drug Administration | FDA Office of Dietary Supplement Programs | dietary supplements | dietary supplement regulation | Dietary Supplement Research Practicum | NIH Office of Dietary Supplements | Mary Frances Picciano Dietary Supplement Research Practicum | NIH | National Institutes of Health |
