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Resources >> White papers >> Selling Dietary Supplements in U.S.A.

Selling Dietary Supplements in U.S.A.

The global regulatory landscape for dietary supplements varies by regions but generally includes rigorous testing and certification processes to ensure product safety and quality.

In the United States, the FDA enforces regulations such as 21 CFR111 and more recently 21 CFR 117 which outline current Good Manufacturing Practices (cGMPs) for dietary supplements. Download this paper to find out what you should be aware of when selling dietary supplements in U.S.A.

Download the paper now! 

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