Amazon’s latest policy to require third-party testing of supplements may lead to consolidation, disproportionately impacting small business, according to market, regulatory and financial experts.
CBD is being linked with a growing number of compelling health benefits for athletes, and while the emerging science is promising, it comes with a high risk of unintentional doping, nutrition researcher Professor Graeme Close warned in a recent webinar.
The mega retailer's recently issued third-party testing policy is applauded by diverse stakeholders because it fosters trust among supplement consumers, they say.
Finalizing FDA’s massive reorganization to create a unified Human Foods Program under one leader is the “number one” priority ahead of the November presidential election, which could impact the agency’s focus if a new administration wins office, agency...
U.S. District Judge Joan Azrack in the Eastern District of New York has agreed to the schedule for hearings between the Natural Products Association (NPA) and the New York Attorney General regarding ongoing efforts to stop the state’s highly restrictive...
More state and federal legislation is needed to regulate synthetic 'kratom' as it continues to proliferate in the U.S. market, according to a group of scientists and industry advocates.
“Oftentimes it feels like we are the first in our industry to ask some of these questions of our supply chain, there isn’t a playbook yet to use,” said Lindsay Dahl, Ritual's Chief Impact Officer.
Top takeaways from regulatory session at SupplySide East
The U.S. Food & Drug Administration's good manufacturing practice (GMP) inspections of dietary supplement facilities is back up to 500 per year, a return to pre-COVID levels, but those levels are still inadequate, says Dr. Cara Welch, FDA’s director...
“From both a consumer standpoint and from an industry standpoint, it's very hard to know what you can and can't do [with kratom],” industry lawyer Rick Collins told attendees at SupplySide East 2024.
FDA’s director of the Office of Dietary Supplement Programs (ODSP), Cara Welch, PhD, stopped by SupplySide East to present an overview of the agency’s FY23 activities related to dietary supplements and FY24 plans as well as an update on the pending Human...
A judge in the Southern District of New York has denied the Council for Responsible Nutrition’s motion for a preliminary injunction against a new law coming into effect on Monday, April 22 that will restrict access to certain dietary supplements for people...
When it comes to starting a dietary supplement brand from scratch, there is a lot to consider: suppliers, contract manufacturers, regulations, supply chain and so much more. So where should entrepreneurs start?
SupplySide East just wrapped up, and attendees were buzzing about a number of issues ranging from restrictive laws to NDI guidance to DSHEA. NutraIngredients-USA caught up with CRN’s President and CEO Steve Mister Wednesday in Secaucus, NJ to discuss...
South Carolina Congressman Jeff Duncan has written to FDA Commissioner Dr. Robert Califf asking for clarification on several dietary supplements issues, including a perceived lack of a response from the Agency to test results from NOW Health Group of...
Registration is open for the DSHEA Summit, a landmark event bringing together the architects of the law and leading industry voices, including current and former FDA officials.
FDA is seeking additional authorities and funding in its fiscal 2025 budget request to enhance its oversight – and by extension safety enforcement – of new food ingredients, additives and contact materials as well as dietary supplements.
In a letter addressed to U.S. Senator Richard Durbin (D-IL) dated March 26, 2024, the National Products Association (NPA) reiterated its continued objection to the re-introduction of the Dietary Supplement Listing Act.
Loren Israelsen, president of the United Natural Products Alliance (UNPA) and one of the key architects of the Dietary Supplement Health and Education Act (DSHEA), is urging the Food and Drug Administration (FDA) to “move along as quickly as they can”...
The National Football League (NFL) is partnering with Canadian researchers on a clinical trial to test the safety and efficacy of CBD for pain management and neuroprotection from concussions.
New York’s law, which prohibits retailers in the state from selling certain dietary supplements to consumers under age 18, lacks clarity and creates confusion for consumers, retailers, marketers and manufacturers, explained Steve Mister, president &...
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.