NPA filed comments with the Food and Drug Administration regarding its review of “Responsible Innovation in Dietary Supplements.”
NPA’s comments follow the recent passage of legislation in the House of Representatives today that would appropriate $100,000 for FDA to perform a Health Hazard Evaluation (HHE) and set a safe level of CBD for consumers to use each…
“Jim grew up on a farm in Indiana learning the basics of design and management of food manufacturing and distribution and now he runs some of the top supplement operations in North America,” said NPA's Dan Fabricant, Ph.D.
Dr. Martin Kullen, DuPont’s research and development (R&D) lead for probiotics, fibers and HMO and Microbiome, and Amy Smith, Regulatory Global Lead for DuPont probiotics, will speak at the Natural Products Association’s “The Big Natural”.
Appropriates Funds Instructing FDA to Conduct Health Hazard Evaluation
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