“We always want to be ahead of what our customers needs are in terms of capabilities, capacity, and technology,” says Mark Wright, founder and president of Health Wright Products.
The International Association of Athletics Federations (IAAF) makes available an updated guide containing to sports nutrition as part of its consensus statement designed for athletes.
Facilities that are subject to FSMA inspections are struggling with the initial implementation of the Foreign Supplier Verification Provision of the law, new data shows. The issue is coming to a head with the first warning letter based on a FSVP failure.
Biotech firms are reaping the rewards of a project looking into foods tackling metabolic syndrome resulting in products like microalgae, omega-3 and antioxidant-infused juices and algae-derived omega 3 oil.
This year’s edition of the Council for Responsible Nutrition (CRN)’s annual Day of Science in Carlsbad, CA, will examine healthy aging and advances in nutrition research tools.
When Adel Villalobos first entered the nutraceutical industry, he noticed that contract manufacturers often “held brands hostage.” He started his own contract manufacturing company with a goal of being different.
New Jersey-based ingredients specialist PLT Health Solutions launched a Certified for Sports Grade version of its branded Rhodiola rosea, called RhodioLife, to the US market.
FDA should issue targeted guidances to facilitate the filing of New Dietary Ingredient Notifications, according to comments filed by the American Herbal Products Association.
Could a simple picture taken on a phone really authenticate chopped or powdered herbs that look identical? Yes, says the co-founder of BriteScan, a potential new weapon in the verification arsenal.
Researchers from global testing firm Eurofins and lab equipment company MilliporeSigma test a “simpler, less time-consuming, and more economical” method of quality control and determination of four bioactive types of vitamin B12.
Vitaquest International, a nutrition industry contract manufacturer, announced this week that it will lease a new manufacturing site in in Parsippany, NJ. Its CEO says it is “the most significant investment in the history of our company.”
Dynamine, a branded form of methylliberine distributed by California-based ingredient company Compound Solutions, has gone through the self-affirmed Generally Recognized as Safe (GRAS) process to validate its safety.
Supplement brand Nature’s Way announced yesterday that 300 products in its herbal line will now come in packaging made up of 97% post-consumer recycled plastics.
Lessons learned from the history of the dietary supplement industry can be applied to the hemp world, and the blitzkrieg-like pace of the industry means we’ll know in short order who’s getting the message and who isn’t. It will also put pressure on regulators...
New Jersey-based contract manufacturer Vitaquest International received food safety standards certification by global certifying body DNV GL Business Assurance.
Presentations at the recent FDA meeting on CBD outlined the concerns some academics in the field have about the quality and safety of the products that are on the market.
A joint webinar put on by Global Organization of EPA and DHA Omega 3s (GOED) and the United Natural Products Alliance (UNPA) will help companies understand the intentional adulteration provisions of FSMA.
There’s a finite supply of ingredients in the natural products industry, a challenge that one pharma ‘track and trace’ expert wanted to tackle head-on by starting the blockchain company TagOne.
The main purpose of the Botanical Safety Consortium, a public-private effort bringing together stakeholders in the botanical supplements space, is “advancing the science of botanical safety evaluation, [and is] not involved in regulatory decisions or...
A study published recently has found a level of liver toxicity for CBD, putting up a big caveat to the notion within the hemp/CBD world that its products have nothing in the way of safety concerns.
New Jersey-based Vitaquest, a firm that develops and manufactures nutraceutical products, has launched an initiative to highlight the procedures the company follows to assure its quality.
New benchmarking standards developed by the Supplement Safety and Compliance Initiative (SSCI) are being widely welcomed by dietary supplements stakeholders, with the initiative coming up for discussion this week during a key ANSI meeting.
FDA’s new Acting Commissioner of Food and Drugs, Norman Sharpless, promised last week that he will pick up where outgoing Commissioner Scott Gottlieb left off in strengthening nutrition policy and regulation to improve the public’s health and implementing...
Growth in the demand for dietary supplement formulation services has created opportunity for equipment suppliers, including GEMCO, a longtime manufacturer of blenders and vacuum drying equipment based in Middlesex, NJ.
While much of the focus around DSHEA was on Capitol Hill and the machinations of government, an important behind-the-scenes contribution came from the short lived Natural Products Quality Assurance Alliance. But what was NPQAA and how did it help?
Setting firm commodity prices will be one brick in the wall of a fully legitimized hemp industry. One company has set about doing so with a proprietary trading platform.
FDA has reiterated its enforcment stance on CBD and hemp products, has updated a Q&A document on the subject and has specified what kind of information it is seeking in the runup to a public meeting on the subject in May, all as part of documents...
FDA has sent three companies marketing CBD products warning letters over disease claims. The warnings are the first issued under FDA’s de facto ‘enforcement discretion’ policy, which will be discussed at a meeting on CBD set for the end of May.
The new Supplement Safety and Compliance Initiative standards were formally unveiled by late last week at a meeting hosted by Walmart. The standards now go into a 30-day comment period.
A paper published by a group of medicinal biochemistry researchers provides a comprehensive look at the challenges of selecting well characterized materials for testing, including a list of recommendations for best practices.
The world of hemp and CBD products sits at a critical moment in its history, much as the dietary supplement industry did a quarter century ago, according to one of the experts who was there at the birth of the industry.
The splits in the organic movement have given birth to a new initiative to regain the soul of the concept, according to an executive with a major retailer.
Manufacturers can now get a gap assessment as to where they stand under the new GRMA standards, which apply to dietary supplements and other product categories.
By FROM THE EDITOR'S DESK: Confusion in the certification game
Do certifications within the supplement industry provide meaningful information to consumers? Or are they just a way to make a confusing market even more impenetrable?
Bodybuilding.com’s John Venardos shares some of his ideas to improve the regulation of the dietary supplements industry, from better transparency to greater FDA staff accountability, and how to level the playing field.
Alkemist also announces reduction in turnaround time for routine tests
Third party botanical ID test results from Alkemist Labs are now available at ingredientsonline.com for select botanicals, as the online ingredient platform continues to push the transparency envelope.
On Monday FDA Commissioner Scott Gottlieb put forward some ideas about where the regulation of dietary supplements should go in the coming years. This is an opportunity that should not be missed. What should be tops on the industry’s wish list?
Serious adverse events represented only a tiny fraction of overall reports in a detailed look at data from two major dietary supplement manufacturers, according to a recent study.
CBD products are all the rage in the pet supplement world. But these products occupy a similar legal limbo in this realm as they do in supplements meant for humans, experts say.
Nuritas and Pharmavite have entered into a partnership that uses Artificial Intelligence (AI) to discover bioactive peptides that promise a more targeted approach to dietary supplementation.
The Food and Drug Administration has announced a regulatory framework for precertifying medical device software to streamline the way in which these devices are brought to market.
The supplement industry has an opportunity to make a powerful case about its self regulatory capabilities during the interregnum of federal regulatory authority imposed by the budget impasse.
The federal government shutdown has thrown a wrench into the works of the Food and Drug Administration. While food safety might not have been compromised, many of the agency’s more routine assignments are on hold and it may take months to catch up.
