More than half (56%) of dietary supplement professionals said they haven’t read the Aug. 11 NDI guidance—and 6% said they haven’t read it, but told their boss that they did.
The drive toward shorter, cleaner labels and the oft-mentioned dearth of innovation in the supplement sphere are both factors of the maturation of the dietary supplement and functional foods industries, according to one expert.
By By Adi Menayang at the Rocky Mountain Dietary Supplement Forum in Boulder, CO
Loren Israelsen, President of the United Natural Products Alliance (UNPA) called the current auditing landscape of the dietary supplements industry as “redundant, expensive, and inconsistent”
Plant extract company Mazza Innovation Ltd. has achieved NSF Good Manufacturing Practice (GMP) registration for its Delta, British Columbia botanical extraction facility.
The long term stability of Rimfrost’s Pristine krill powder at room temperature has been confirmed in two studies, allaying concerns about krill’s viability as a supplement ingredient due to stability issues.
Nine companies are beta-testing the CRN’s product registry – the Supplement Online Wellness Library (Supplement OWL) – which is being developed and administered by UL.
The new NDI draft guidance is very similar to the previous version, and yet the howls of outrage heard in 2011 are silent. What’s changed? Well, a lot…
Consulting firm Ingredient Identity has launched an outsourced quality assurance solution that could help smaller companies demonstrate better—and more cost effective—compliance in this important function.
The dietary supplements industry has done a great job coming together to address raw material supply in the wake of the New York Attorney General’s action, says George Pontiakos, CEO of BI Nutraceuticals.
Demand for Frutarom’s HyperPure ingredients is growing twice as fast as its non-HyperPure since the beginning of 2016, linked to a diminishing consumer trust in supplements and the call for short ingredient lists, says the company.
Gisele Atkinson has joined the Council for Responsible Nutrition as the vice president, quality and technical affairs, a new position in the association’s science and regulatory department.
The Natural Products Association (NPA) has announced the launch of its warning letter database, giving access to data on GMP violations, technical adulteration, and labeling infringements.
DNA barcoding to identify and authenticate botanical ingredients in dietary supplements should only be used in addition to other existing analytical methods, says a new expert review.
Despite the tenor of a recent meeting of ex FDA commissioners, DSHEA didn’t tie the hands of federal regulators, experts contacted by NutraIngredients-USA have said.
The botanical raw material GMP proposal put forward by GNC earlier this year is in active revision, according the American Herbal Products Association.
Is the dietary supplement industry getting a handle on the adulteration issue? The baseline data does not exist to be able to say one way or another. But sources agree that in the one thing you can measure—the attention the issue is getting—the situation...
Despite support from a prestigious Cochrane Review, many manufacturers to re-emphasize chondroitin and to use efficacious amounts in their supplements, says the President and CEO, Synutra Pure.
Boswellia serrata adulteration remains a major problem in the EU and elsewhere and responsible players need to do more to identify fraudulent material and actors, an expert has said.
Schneiderman, McCaskill, Cohen, Frontline… it’s been blow after blow for the dietary supplements industry, so you have to ask if consumer confidence and trust in the products have been affected.
A warning letter to a company called Rocky Fork Formulas has particular insights for the labeling operations in the dietary supplement responsibility chain.
The US Food and Drug Administration is developing a next-generation toolbox for analyzing live microbial products, including DNA microarrays, metagenomic sequencing and analysis, and a whole genome database development.
The ABC-AHP-NCNPR Botanical Adulterants Program has announced the publication of a new series of reviews on adulteration of botanical ingredients called the Botanical Adulterants Bulletins (BABs).
With the recent elevation of dietary supplement oversight from a division to its own office at FDA’s Center for Food Safety and Applied Nutrition, the agency should renew its focus on reducing tainted supplements, improving compliance with good manufacturing...
Eighty-one percent of responders to a recent UNPA survey think the dietary supplements industry would need a new quality seal if the industry had to move toward a single seal of quality, a result that should serve as a wake-up call to the existing and...
Lab reports that mimic Alkemist Labs’ distinctive testing format may be causing confusion in the marketplace and undermining the integrity of an Alkemist Labs C of A, the company has said.
Two new studies have shown what many in industry have been claiming for a long time: DNA barcoding by itself is not an adequate method for analyzing botanical dietary supplements.
The US Food and Drug Administration tells NutraIngredients-USA that it looks forward to learning more about the Council for Responsible Nutrition’s proposed industry-wide dietary supplement product registry.
The Council for Responsible Nutrition’s Board has unanimously authorized the creation of an industry-wide dietary supplement product registry to be launched by the end of the year.
DNA testing and verification of seaweed can be useful in an increasingly busy sector where quality varies and manufacturer demands are rising amid stricter regulations, an aquaculture group has said.
A newly updated AHP monograph on cranberry identification will set a new standard in ensuring the quality and efficacy of this botanical, said one of the paper’s co-authors.
Experts from the US FDA, EFSA, Food Standards Australia New Zealand, and Anvisa will provide regulatory insights about global probiotic regulations at the 2016 IPA World Congress + Probiota Americas.
Supplement heavyweight GNC’s industry initiative to boost supply chain integrity and defend consumer confidence is gaining momentum, with over 80 different companies involved in the consortium to date, said the company’s CEO.
“A waste of money”, “not subject to testing by the FDA”, and “made from untested synthetic chemicals from China” are just some of the points made by Attorney General Loretta Lynch in a new video.
Mazza Innovation Ltd has formally opened its commercial-scale processing facility featuring its proprietary water extraction technology branded as PhytoClean.
Herbal medications and supplements are lacking clear proof of any beneficial effects, except cranberry for UTIs, states a new Patient Page in the Journal of the American Medical Association (JAMA).
Trying to solve the supply chain issues facing the dietary supplement industry is complicated by the muddled state of documentation practices, but there are efforts underway to address the problem.
China’s food authorities are unable to keep up with cases of chemical and drug adulteration, according to the head of its Food and Drug Administration.
After years of hand wringing over the situation in raw material supply in which low quality ingredients find a home in the marketplace, consensus now seems to be building in the dietary supplement industry to do something about it. But at a recent industry...
Three of the trade organizations representing the dietary supplement business came together in Utah this week to lend support to plans to extend the industry’s self regulation capabilities.
GNC’s new raw material GMPs, announced as a final intent if not in final form at an industry event this week, is “a concept whose time has come,” according to CEO Mike Archbold.
GNC has announced a GMP plan for botanicals which it is implementing immediately for its suppliers. The company hopes the plan, announced at an industry meeting on Tuesday, will become a blueprint for the industry.
The New York Attorney General’s controversial probe into dietary supplements has hastened the conversation about transparency, experts told attendees to our recent Transparency in Dietary Supplements forum.
The quality and consistency of dietary ingredients and supplements would improve by “universal adoption” of the USP–NF science-based public standards, says a new paper.
A major product liability provider is exiting the dietary supplement field, but observers of insurance trends said it’s unlikely to have big impact on insurance rates or availability.
Transparency in the supply chain rests on reliable tests to verify the provenance of ingredients, but proving beyond doubt where an oil came from has been a problem in the omega-3s space. A new test method being brought to market by the company OmegaVeritas...
