Twenty Years of the Dietary Supplement Health and Education Act—How Should Dietary Supplements Be Regulated?  

Oleh:

Wallace, Taylor C

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: JN: The Journal of Nutrition vol. 145 no. 08 (Aug. 2015), page 1683-1686.
Topik: Dietary Supplement Health and Education Act dietary supplement regulation structure/function claim premarket approval adverse event reporting current Good Manufacturing Practices

Ketersediaan

Perpustakaan FK Nomor Panggil: J42.K Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

The Dietary Supplement Health and Education Act (DSHEA) of 1994 defines the FDA’s statutory authority to regulate dietary supplement products in the United States. The dietary supplement industry has rapidly expanded since 1994, presenting an obvious need for “DSHEA 2.0.” Current regulations surrounding dietary supplements have been increasingly and reasonably scrutinized, given their widespread use by over one-half of the US population as well as highly publicized safety concerns over the past 20 y. As the market continues to expand and evolve, so too must the laws that protect consumers from potential harm and misleading communication. This article is meant to begin a scientific dialogue on how regulations may be improved to provide both ease of access and safer products to the consumer by focusing on 4 topics: premarket approval, label claims, current Good Manufacturing Practices, and adverse event reporting.

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