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Daniel Fabricant


FDA Asks for Consumer Input on Labeling Plant-Based Products, NPA Responds

by Shari Barbanel | October 4, 2018

The U.S. Food and Drug Administration (FDA) has issued a request for information as it examines its approach to the use of dairy food names like “milk,” “cheese,” or “yogurt” in the labeling of plant-based foods and beverages. Earlier this year, FDA Commissioner Scott Gottlieb announced FDA’s Nutrition Innovation Strategy (NIS) in a speech to the National ...

Study Advocates for Risky FMT Procedure Over Probiotic Supplements

by Nicholas Saraceno | September 11, 2018

A new study published in the medical journal Cell encourages patients to avoid probiotics in favor of a medical procedure that is known to cause adverse events in more than 25 percent of patients. The Natural Products Association (NPA) pointed out the near universal medical consensus that probiotics are safe and effective and questioned why ...

Trump Tariffs Will Impose Financial Burden on Supplement Industry, NPA Warns

by Shari Barbanel | July 30, 2018

The Trump Administration’s proposal to impose tariffs on key ingredients for nutritional supplements and vitamins will cause disproportionate economic harm to U.S. interests and increase costs for small businesses and consumers, the Natural Products Association (NPA) said in a letter to United States Trade Representative Robert E. Lighthizer.  President and CEO of NPA Daniel Fabricant, ...

Study Questions Importance of Supplements, Industry Responds

by Shari Barbanel | May 30, 2018

Nutritional supplement industry associations have responded to a new study led by researchers at St. Michael’s Hospital and the University of Toronto, which suggests that the most commonly consumed vitamin and mineral supplements provide no consistent health benefit or harm, and says to rely on a “healthy” diet for vitamins and minerals. Published in the ...

NPA to Hold “The FDA Experience” Training Event

by Shari Barbanel | June 28, 2017

The leading experts in the field of the natural products industry and former U.S. Food and Drug Administration (FDA) officials Daniel Fabricant, PhD, president and CEO of Natural Products Association (NPA) and Corey Hilmas, MD, PhD, NPA’s senior vice president of scientific and regulatory affairs, will host a five-day training dubbed “The FDA Experience” on ...

Natural Industry Primes for Amazon

by Shari Barbanel | June 20, 2017

By Janet Poveromo On June 16, Amazon announced its plan to acquire Whole Foods for $42 a share, in a deal valued at $13.7 billion. Whole Foods’ John Mackey will remain CEO of the grocery store chain and the deal is expected to close in the second half of the year. The news sent shock ...

NPA Modernizes and Strengthens Bylaws

by Shari Barbanel | February 28, 2017

The Natural Products Association (NPA) has announced the approval of new bylaws that will govern and steer the organization into the future. The new bylaws were approved by the full membership on February 17, 2017. “NPA has being growing and doing more with less over the last three years. In order to sustain that growth ...

NPA Supports Lawful Marketing of Vinpocetine

by Shari Barbanel | November 8, 2016

The Natural Products Association (NPA) has submitted comments to the U.S. Food and Drug Administration (FDA) in response to the agency’s recent actions to ban vinpocetine. FDA is collecting public comments following a Federal Register notice that would effectively ban vinpocetine, a widely used product found in safe and legal dietary supplements. The FDA’s decision ...

NPA Keeps Up Pressure on Puerto Rico Over New Fees

by Shari Barbanel | September 12, 2016

The Natural Products Association (NPA) recently urged the Congressional Task Force on Economic Growth in Puerto Rico to highlight the damaging effects of Administrative Order 346, which established barriers to retailers and distributors of natural products in Puerto Rico through new fees and unnecessary regulations, making it difficult for products to reach consumers. The Task Force is scheduled ...

FDA Considering Vinpocetine Ineligible as a Dietary Ingredient

by Shari Barbanel | September 9, 2016

The U.S. Food and Drug Administration (FDA) recently released an unprecedented Federal Register (FR) notice (Docket No: FDA-2016-N-2523) with major implications for acknowledged new dietary ingredient (NDI) notifications. FDA appears to be attempting to shift the burden of demonstrating reasonable expectation of safety for vinpocetine on the industry by using the hook that it can’t ...

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