Michael McGuffin
FDA, Stakeholders Meet, Mull Over Pre-DSHEA Dietary Ingredients List
On October 3, the U.S. Food and Drug Administration (FDA) held a public meeting to discuss the development of a list of pre-Dietary Supplement Health and Education Act of 1994 (DSHEA) dietary ingredients. According to a release from Washington, D.C.-based law firm Keller and Heckman LLP, the meeting featured two stakeholder panels that presented on ...
Associations Submit Comments on Revised NDI Draft Guidance
Some of the natural product industries’ leading associations, including the American Herbal Products Association (AHPA), Council for Responsible Nutrition (CRN), American Botanical Council (ABC) and Natural Products Association (NPA), recently submitted comments to U.S. Food and Drug Administration (FDA) in response to the agency’s revised New Dietary Ingredient (NDI) Draft Guidance. FDA issued on August ...
AHPA Issues Slack-fill Guidance
The American Herbal Products Association (AHPA) has published slack-fill guidance to help the regulated supplement industry inform consumers and comply with all relevant federal requirements. The difference between the capacity of a container and the volume of product inside is known as “slack-fill.” The U.S. Food and Drug Administration (FDA) regulates how food (including dietary ...
Wilson Lau to Chair AHPA Board of Trustees
The American Herbal Products Association (AHPA) Executive Committee has appointed Wilson Lau as chair of the AHPA Board of Trustees until March 2017. Lau is the vice president of sales at nuherbs Company and has served on the AHPA board since 2008. He is also chair of AHPA’s Tea and Infusion Products Committee. “AHPA appreciates ...
Industry Urges FDA to Define “Natural”
The American Herbal Products Association (AHPA) submitted comments to the U.S. Food and Drug Administration (FDA) encouraging the agency to establish, through rulemaking, a regulatory definition for the term “natural” (and possibly other terms, such as “100 percent natural” and “made with natural [named ingredient(s)]”) for the labeling of human food products, and other products ...
Senator Blumenthal Withdraws Amendment to Limit Military Access to Supplements
Senator Richard Blumenthal (D-CT) withdrew his amendment to the FY 2017 National Defense Authorization Act (NDAA) that would require supplements sold on military bases to be verified by a third-party amid strong opposition by the supplement industry. Enacted on an annual basis by Congress, NDAA legislation establishes budget and policy parameters for the Department of ...
Frontline Segment: Skewed & Misleading, AHPA Says
A segment aired on January 19 on PBS’ Frontline presented dietary supplements as inherently unsafe by misrepresenting the rigorous safety provisions established for these products under the Federal Food, Drug and Cosmetics Act, the strict liability statute under which supplements are regulated. The segment, titled “Supplements and Safety,” relied on anecdotal reports of noncompliant products ...
The Path to Compliance
To rebuild consumer trust, the natural products industry must exhibit compliance and transparency. The issue of compliance has affected many aspects of the natural products industry. Nutrition Industry Executive (NIE) magazine asked those schooled on the subject to discuss this topic, and offer their thoughts on what the industry can do to make safe products, ...
Industry Roundtable: The Path to Compliance
The issue of compliance has affected many aspects of the natural products industry. Nutrition Industry Executive (NIE) asked natural product industry experts to discuss this topic, and offer their thoughts on what the industry can do to ensure safe products that comply with government regulations and help gain the confidence of consumers. The Participants Are: ...
NPA and AHPA Support FDA Efforts on Adulterated Dietary Supplements
The Natural Products Association (NPA) has made it very clear that it will crack down on manufacturers selling adulterated products. Daniel Fabricant, PhD, executive director and CEO, NPA, who was the former director of the Division of Dietary Supplement Programs at the Food and Drug Administration (FDA), commented on a new report in The Journal of the American Medical Association (JAMA), in which ...
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