The Dietary Supplement Innovation Act, introduced by Rep. Harshbarger, would cap indefinite preclusion, require science-based review standards, and open FDA warnings to court challenge.
|Articles|June 27, 2011
Draco Passes GMP Inspection
The San Jose-based botanical extract supplier recently passed a Good Manufacturing Practices (GMP) inspection conducted by SGS.
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“As a supplier of botanical ingredients, it is not a direct requirement for us to have cGMPs in our processing facility, but it is a requirement for many of our customers.”
In addition to Draco’s successful GMP inspection, the company offers other certifications, including National Organic Program (NOP) and EU organic certification and kosher certification.
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At the Future Nutra Innovation Summit, Sibyl Swift, PhD, founder and principal of Swift Strategy Group, discusses supplement oversight and unpacks why mandatory product listing divides the industry.
The inaugural Future Nutra Innovation Summit opened with organizers pitching a networking-first alternative to the traditional trade show, followed by an NSF presentation on certification failure rates and consumer trust that set a tone for the rest of the event.
This overview outlines the clinical background, consumer landscape, and technical developments shaping the gluten-free category.
A new request for information, expert roundtable findings, and a transatlantic workshop signal FDA's renewed focus on plant-based drug products.
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