By Daniel Fabricant, PhD, President & CEO, Natural Products Association
In this guest column, the Natural Products Association's Dr. Daniel Fabricant outlines his organization's opposition to FDA's proposal for a mandatory product listing for all dietary supplements.
The U.S. Food and Drug Administration has outlined its budget and legislative proposals for 2025, with the only dedicated section concerning dietary supplements renewing calls for mandatory product listing and seeking clarifications on the Agency's...
While FDA may not be able to assess the safety of as many chemicals in the food supply as it or the public would like due to budget constraints, the agency last week pulled back the curtain slightly to reveal which chemicals it is reassessing, how they...
Connecticut lawmakers once again seek to ban the sale of energy drinks to consumers younger than 16 years, as regulators and researchers raise concerns about the negative health impact of caffeine.
Experts speaking at this year’s Sports and Active Nutrition Summit expressed concern that New York, California, Massachusetts and a growing number of states are moving to restrict access to the use of weight loss and muscle building supplements by minors.
FDA's final guidance on New Dietary Ingredient (NDI) notification procedures and timeframes has prompted a range of responses from the dietary supplement industry trade associations, with some more welcoming than others.
FDA will not object to two qualified health claims linking consumption of yogurt and reduced risk of type 2 diabetes, regardless of fat or sugar content, but in an enforcement discretion letter to Danone North America detailing its decision the agency...
The Food and Drug Administration (FDA) has finalized guidance for industry titled “Dietary Supplements: New Dietary Ingredient Notification Procedures and Timeframes: Guidance for Industry".
Yogurt brands will be able to leverage a scientifically-backed health claim for the first time thanks to a successful petition lodged by Danone North America.
FDA's massive reorganization to create a unified Human Foods Program under one leader who reports directly to the agency’s commissioner may take longer than originally anticipated, but is “going quite well,” the program’s first Deputy Commissioner...
Food law expert Dr Mark Tallon, of the UK-based food law firm Legal Foods and the Food Law Academy believes a key skill missing for professionals in the food industry is a strong understanding of the threats and opportunities surrounding intellectual...
The dietary supplement industry has come a long way. A significant number of new dietary supplement products have appeared in the marketplace since Congress passed the Dietary Supplement and Health Education Act (DSHEA) of 1994. At that time, there were...
The Council for Responsible Nutrition is calling on the U.S. Food and Drug Administration (FDA) to act against products formulated with the Alzheimer drug galantamine and marketed as dietary supplements .
A multi-year case involving dietary supplement startup PPO Lab, the Federal Trade Commission (FTC) and COVID-19-related health claims has come to a close, culminating in a truce that removes fines and lightens administrative burdens on the defendants.
Even as FDA stands by its decision that CBD is not safe for use in foods, beverages and dietary supplements, the agency is considering how best to ensure it is clearly labeled, safely manufactured and consumers understand what it is, according to a senior...
A new paper is out titled “Safety Considerations for Dietary Supplement Manufacturers in the United States", co-authored by Jay Sirois, PhD, VP of regulatory and scientific affairs, Consumer Healthcare Products Association, alongside several CHPA...
The issues that restrict the sale of supplement ingredients in the United States and the European Union surround similar battles between federal and state control, according to a new analysis published in the Journal of Dietary Supplements.
As states continue to pass bills to restrict the sale of weight loss and muscle building supplements to minors, new research shows how a little education goes a long way.
Industry experts propose the creation of a new executive position within organizations to help combat a rise in Food and Drug Administration citations against supplement companies who don’t meet quality control standards.
The Chambers-ranked attorney provides regulatory counseling and litigation support to brands marketing consumer products, including cosmetics, personal care products and dietary supplements.
With what feels like a weight loss medication takeover, many are betting that the GLP-1 receptor agonists will rescue America from its obesity epidemic. So what does this mean for the natural weight loss products?
Italy has introduced new advertising guidelines for social media influencers which will see the most influential online celebs regulated by the same authority as mass media outlets.
There is still time to register for our Annual Business Leaders Forum, and your chance to ask a burning question (or two) to senior leaders from Gaia Herbs, Nouri, NOW, Pharmavite and The Vitamin Shoppe.
The Association for the Cannabinoid Industry (ACI) has published a report calling on the UK Food Standards Agency (FSA) and the Home Office to work together to end the regulatory stalemate threatening the sector.
The supplements labeled as weight loss products appear to be mislabeled as testing revealed the tejocote root was substituted with a potentially deadly plant.
The U.S. Food & Drug Administration has warned Amazon about “energy enhancing supplements or foods” alleged to contain undeclared sildenafil and tadalafil for male sexual performance.
Apex Compliance entered the dietary supplement space to simplify regulatory compliance by helping companies identify the words and phrases across marketing materials that trigger oversight agencies.
The 4th Annual Business Leaders Forum will take place on January 25. The FREE webinar gives attendees the opportunity to ask a burning question (or two) to our C-suite panel from some of the most iconic brands in the dietary supplements space.
By Steve Mister, President & CEO, Council for Responsible Nutrition
As my grandmother used to say, “You get more flies with sugar than you do with vinegar—but a good bug zapper will do the job sometimes too.“ Yes, she was a wise and pragmatic woman.
By Loren Israelsen, Founder & President, United Natural Products Alliance (UNPA)
My reflection on 2023 has little to do with specifics. In my view, this was a year of opposite choices and opposing directions – the big stuff. Yet, daily demands to address the urgent (but often not so important) dulled our senses and intuition. Hence,...
Natural products manufacturer NOW has reported that dozens of "no name" berberine supplements sold on Amazon and Walmart.com do not meet potency claims on label.
By Daniel Fabricant, PhD, President & CEO, Natural Products Association
It's become too commonplace and cliché to state that the world is very different now than it was just a few years ago. Heck, 2023 is very different at the end than how it began.
From the state of the market to the impact of inflation, mega trends like mushrooms and women’s health, the TikTok effect, working with influencers and brand ambassadors, the NutraIngredients-USA’s Business Leaders Forum will dig deep into a range of...
The future of self-care is a multifaceted landscape that hinges on access, continued innovation, and a collective effort spanning input from consumers, communities, healthcare providers, regulators, and policymakers.
As caffeine content in energy drinks climbs to new heights, some countries and retailers are banning the products or imposing age restrictions. In the US and UK, there are no national regulations that ban the sale of highly-caffeinated energy drinks,...
Dr Cara Welch, Director of FDA’s Office of Dietary Supplements Programs, and Christine Burdick-Bell, EVP & General Counsel at Pharmavite, have confirmed their participation in the NutraIngredients-USA’s landmark DSHEA Summit.
By Michael McGuffin, President, American Herbal Products Association (AHPA)
As 2023 comes to a close, so too does another year of progress and innovation in the dietary supplement and natural product industries that the American Herbal Products Association (AHPA) proudly serves. The growth of newer product categories – such as...
Before coming to Clean Label Project, Jackie Bowen held numerous technical, standards development, food safety, quality, and executive roles within the World Health Organization Collaborating Centre, NSF International. Her expertise is in organic, gluten-free,...
Andrea Wong, PhD, senior vice president of scientific and regulatory affairs at the Council for Responsible Nutrition, responds to emerging issues and is a major advocate for science-based nutrition.
A new publication from BfR, the German Federal Institute for Risk Assessment, concludes that omega-3 fatty acid supplements may increase risk of atrial fibrillation in those with existing or impending heart disease, with the greatest risk noted at the...
A federal court has ordered the manufacturer and distributor of the Balance of Nature brand to cease the production and sale of the dietary supplements after the FDA accused the two Utah-based companies behind it of multiple violations spanning years.
Dietary supplement trade associations headed to Boston this week to provide testimony in opposition to bills that would restrict access to weight loss and sports nutrition dietary supplements for consumers under the age of eighteen.
FDA’s massive reorganization to create a proposed unified Human Foods Program under one leader who will report directly to the agency’s commissioner may not be finalized until next June, but the program’s first Deputy Commissioner James ‘Jim’ Jones isn’t...
By Steve Mister, President & CEO, Council for Responsible Nutrition
In this guest article, Steve Mister, President & CEO, Council for Responsible Nutrition, discusses how “surgical amendments to the existing drug preclusion provision” can balance the interests of drugs and supplements and allow innovation in both...
After decades of navigating the complexities of regulatory compliance, Emma Hunt and Kathryn Szymonowicz took their knowledge and used it to launch Rubicon Bridge, a software that helps other businesses to overcome regulatory challenges and achieve international...
We’ve seen a number of state bills prop up, especially out of California. In fact, at this time last year we were talking about AB 2098, a contentious bill that would have disciplined physicians for spreading misinformation about COVID. That bill was...
For the second time in two months, the US Food and Drug Administration has declined to respond to a Citizen Petition, citing “competing agency priorities”.
