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|July 1, 2009
Cerilliant Introduces Certified Reference Standards for Stevia
Cerilliant (Round Rock, TX), a producer and provider of certified reference standards and materials, announced the introduction of two new certified reference standards today, Rebaudioside A (Reb-A) and multi-component Rebaudioside-A Impurities.
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Cerilliant (Round Rock, TX), a producer and provider of certified reference standards and materials, announced the introduction of two new certified reference standards today, Rebaudioside A (Reb-A) and multi-component Rebaudioside-A Impurities.
These new reference standards will enable producers of Reb-A, a natural sweetener derived from stevia, to meet FDA guidelines for Reb-A ingredients and to attain a consistent flavor profile in the sweetener.
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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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