A year-to-date look at the federal and state measures shaping supplement oversight, access, and classification.
|Articles|September 1, 2010
Sabinsa Gets ISO Certification in India
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Sabinsa’s (East Windsor, NJ) plant near Bangalore, India, has received Bureau Veritas ISO 22000 certification. Earlier this year, the facility was granted current Good Manufacturing Practices (cGMP) certification by NSF International (Ann Arbor, MI).
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A panel at The Outlook on Active Nutrition discussed quality in sports nutrition focused on testing, liability, and what buyers now expect from suppliers.
Trade groups say the law's broad criteria could restrict access to supplements with uses beyond weight loss or muscle building.
Part 2 of our interview with Todd Harrison, co-chair of the FDA practice group at Venable LLP covers preclusion's structural gaps: no defined end point, no tracking registry, and a push for mandatory drug-sponsor engagement.
Todd Harrison, co-chair of the FDA practice group at Venable LLP, details the Dietary Supplement Innovation Act's language, its unintended consequences, and what industry stakeholders should watch for.
Piping Rock Health Products has launched a 300-mg NMN gummy under its Vitafusion brand, arriving less than a year after the FDA reversed its position on whether the ingredient could legally be sold as a dietary supplement.
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