Regulation & policy

Supplement sector rising, ‘safety needs to evolve with it’

NI+Supplement sector rising, ‘safety needs to evolve with it’

By Asia Sherman

Growing supplement use, novel ingredients, personalized nutrition and digital health advice are challenging safety frameworks in a fragmented global regulatory landscape, prompting greater discussion about the tools needed to foster regulatory coherence.

FDA, industry outline priorities for dietary supplement modernization

FDA, industry outline priorities for dietary supplement modernization

By Danielle Masterson

As the US Food and Drug Administration (FDA) considers how to modernize dietary supplement oversight, Cara Welch, PhD, director of FDA’s Office of Dietary Supplement Programs, has emphasized the agency’s commitment to keeping pace with an evolving...

Drug Preclusion: Necessary Reform

Opinion piece

Drug Preclusion: Necessary Reform

By Steve Mister, President & CEO, Council for Responsible Nutrition & Graham Rigby, President & CEO, American Herbal Products Association

Industry agrees that drug preclusion is broken and in need of reform. We all saw what happened with NAC and NMN. And we want dietary supplement companies to have greater certainty before investing millions of dollars developing and marketing an ingredient.

Drug preclusion: Consider the source

Opinion piece

Drug preclusion: Consider the source

By Daniel Fabricant, PhD, President and CEO, NPA

CRN, CHPA and AHPA are celebrating H.R. 10336 as a balanced compromise. But in the pursuit of regulatory certainty, has part of the supplement industry agreed to permanently enshrine the very pharmaceutical gatekeeping mechanism it has spent years fighting?

SANS USA moves to Dallas for 2027

SANS USA moves to Dallas for 2027

By Cassandra Stern

The Sports & Active Nutrition Summit USA (SANS USA) is heading to Dallas in 2027 after two consecutive sold-out editions in San Diego.

Alice Mushrooms case tests limits of ingredient substantiation

Alice Mushrooms case tests limits of ingredient substantiation

By Cassandra Stern

A recent case decision offers a closer look at how the National Advertising Division (NAD) approaches ingredient-level research when companies make claims for multi-ingredient products, including when that evidence can be extrapolated to the finished...

New Jersey legislator introduces restrictive supplements bill

New Jersey legislator introduces restrictive supplements bill

By Stephen Daniells

A lawmaker in New Jersey has filed a bill to prohibit the sale of weight loss and muscle building products to minors, part of a broader trend of state-level efforts to restrict youth access to certain dietary supplements.

What is the industry getting wrong? FNIS leaders weigh in

What is the industry getting wrong? FNIS leaders weigh in

By Danielle Masterson

From social media pseudoscience and influencer culture to industry advocacy and trend-chasing, Future Nutra Innovation Summit (FNIS) attendees outlined where they see gaps — and what could change them.

More protein, more fiber, more questions: What happens to gut health?

NI+More protein, more fiber, more questions: What happens to gut health?

By Marie Latulippe, MS, MBA, RD, Senior Director of Science Programs, Institute for the Advancement of Food & Nutrition Sciences (IAFNS)

Protein and fiber are having a moment, and consumers are being encouraged to get more of both, from fortified foods and functional products to social-media trends and new approaches to weight management.

NutraCast: On the coca trail with the Medicine Hunter

NutraCast: On the coca trail with the Medicine Hunter

By Danielle Masterson

For centuries, coca leaf has played an important cultural and traditional role in the Andes. But outside South America, the plant is far more likely to be associated with one thing: cocaine. So what happens when we separate the coca leaf from the drug...

FDA wants more GRAS oversight – but can it handle the workload?

FDA wants more GRAS oversight – but can it handle the workload?

By Elizabeth Crawford

FDA wants companies to notify the agency when they determine food ingredients are Generally Recognized As Safe. But with hundreds of potential notifications and fewer staff, questions remain over whether FDA has the resources to review them

Supplements 101: What are peptides?

NI+Supplements 101: What are peptides?

By Lauren Nicolle

The surge in GLP-1 drug use has brought peptides from a niche research area into the mainstream, sparking growing interest across nutrition and health, but confusion remains about what they are and how they are regulated.

Qunol faces class action over omega-3 claims

Qunol faces class action over omega-3 claims

By Cassandra Stern

Quten Research Institute is facing a proposed class action alleging that its Qunol Ultra Omega-3 Fish Oil contains less omega-3 than the 1,000 mg advertised on the product label.

FDA proposes mandatory GRAS notifications

NI+FDA proposes mandatory GRAS notifications

By Danielle Masterson

The U.S. Food and Drug Administration is proposing to make the currently voluntary GRAS notification system mandatory, giving the agency greater visibility into substances companies determine are Generally Recognized as Safe.

Bipartisan hemp bill seeks federal pathway for cannabinoid products

Bipartisan hemp bill seeks federal pathway for cannabinoid products

By Cassandra Stern

The proposed legislation would establish a federal regulatory framework for hemp-derived cannabinoid products, which industry stakeholders say could provide long-sought regulatory certainty for manufacturers and create a clearer pathway for nutrition and...