Adverse event reporting for dietary supplements
Manufacturers of dietary supplement products must submit reports of “serious adverse events” to FDA.
Manufacturers of dietary supplement products must submit reports of “serious adverse events” to FDA.
One common myth is that FDA doesn’t oversee or regulate dietary supplement products.
FDA and FTC share responsibility for the oversight of dietary supplements and related promotion.
cGMPs are crucial manufacturing rules to ensure the quality of dietary supplement products.
Nutrient content claims describe the level of a nutrient in the product, using terms such as “free.”
Health claims describe a relationship between a food substance and reduced risk of a disease or health-related condition.
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