EUDR ‘no risk’ status cancelled and 12 month delay reconfirmed
The controversial EUDR no risk status has been provisionally binned in a ‘trilogue’ between the European Council, Commission and Parliament.
News, Analysis & Insights on Nutrition, Supplements, and Health
The controversial EUDR no risk status has been provisionally binned in a ‘trilogue’ between the European Council, Commission and Parliament.
The IPA World Congress + Probiota 2025 is two months away! The three-day conference is the leading event for the probiotics, prebiotics, and microbiome community, and here’s why…
The UK Food Standards Agency (FSA) has taken the next step in regulating Cannabidiol (CBD) products, announcing an update in safety assessments, risk management and compliance protocols.
A lot has happened in the global nutrition industry over the past seven days, so catch up with our weekly round-up of key news from across the Nutraverse.
We look at the latest regulatory announcements happening across Asia-Pacific’s health and nutrition sector, including India’s inter-ministerial committee report on nutraceutical regulations, new updates on modern claims product approval in Malaysia and...
French regulators are proposing significant changes to permissible levels for vitamins and minerals in food supplements, which could see vitamin C limits slashed by almost 80%.
Characterization, demonstration, and documentation are the three main foundations for a new roadmap outlined by experts from academia and industry to achieve the authorization of “prebiotic” in future EU health claims.
The EU botanicals industry is celebrating after the General Court of the EU annulled the prohibition of hydroxyanthracene derivatives (HADs) in Aloe spp.
Ayurvedic herbs, probiotics, CBD, and mushrooms are under scrutiny as the mind health boom means brands must overcome regulatory hurdles, says an industry expert.
Guest Article
Over 80 stakeholders from government, academia and industry gathered recently at the first Southern African Botanical Products Association (SABPA) symposium to discuss best practices to successfully bring compliant ingredients to the world market.
A lot has happened in the global nutrition industry over the past seven days, with a restrictive supplements bill passing the New Jersey Assembly, NZ’s new natural products bill and France’s new online platform for supplements among the headlines. Catch...
As COP29 garners global attention, its focus on food systems continues to grow.
Ingredient regulation in food supplements for maternal and infant health is imperative as novel food applications frequently prioritize approval at the expense of maternal and child considerations, according to a legal expert.
The French Ministry of Agriculture has launched Compl’Alim, a mandatory online system for declaring new supplements.
The Global Retailer and Manufacturer Alliance said it is hoping to increase confidence in product integrity within the supply chain by introducing the Innovative Product Integrity Program.
Guest article
As the EU enters a new policy cycle following the European Εlections and with a new European Commission expected to be fully operational in the coming weeks, ESSNA, the European trade body for sports foods, has launched the policy priorities of the...
A lot has happened in the global nutrition industry over the past seven days, with New Jersey attempting to restrict access to select dietary supplements, Japan’s youth reporting being fatigued and anxious, UK guidance over caffeine in supplements and...
The Food Standards Agency (FSA) has issued new guidance to ensure the safe consumption and production of food supplements containing high levels of caffeine in response to growing health risk concerns.
ADM has announced an agreement to acquire Vandamme Hungaria Kft, along with its associated entities, which operate a 700 metric ton per day non-GM crush and extraction facility in northern Hungary.
The Advertising Standards Authority (ASA) identifies two brands making claims that cannabidiol (CBD) is suitable for consumption by children, but “legal and safe are two different things” according to expert opinion.
The American Herbal Products Association (AHPA) has submitted comments to the United Kingdom Food Standards Agency's (FSA) supporting the safety, usage and science of ashwagandha.
Nutritional ingredients supplier dsm-firmenich announced that the United Kingdom and European Union have approved the company's human milk oligosaccharide (HMO) ingredients—3-FL and a mixture of LNFP-I and 2'-FL—as novel food ingredients.
A recent report from the Heads of Food Safety Agencies (HoA) in Europe raised concerns about 13 ingredients in food supplements, including melatonin, piperine, and curcumin. In this guest article, the European Federation of Associations of Health Product...
Guest article
In this guest article, Luca Bucchini, the Chair of the European Specialist Sports Nutrition Alliance (ESSNA), discusses some of the new Commission's policy ambitions impacting the sports nutrition sector.
With expert speakers confirmed from Ani Biome, the Lawson Health Research Institute, Örebro University, ETH Zurich, dsm-firmenich, Novonesis, IFF, Morinaga, Kerry, and more, the upcoming Probiota 2025 is not to be missed.
Recent Advertising Standards Authority (ASA) rulings against Huel and Zoe for misrepresenting celebrity investor Steven Bartlett's involvement have sparked online debate, prompting calls for the ASA to update its guidelines.
Consumers are turning on ultra-processed foods (UPF), with some calling for a UPF manufacturer tax. But do they yet understand the term and how would a UPF tax impact makers?
Insisting on a high bar in product testing protects both a company’s bottom line and the dietary supplement industry’s long-term success, says Alkemist Labs.
Breaching advertising codes for menopause supplement marketing is not fair to the consumer, says a menopause brand expert.
The nutraceutical industry has thanked Basil Mathioudakis for his determination, wit, extraordinary commitment and great legacy, after he passed away on August 2.
In an editorial published in the Journal of Ethnopharmacology, leading natural product researchers summarized the flaws in the botanical research used by European regulators to question the safety of ashwagandha.
The Advertising Standards Agency (ASA) has made six rulings against brands making anti-anxiety claims, utilizing its new AI monitoring system to catch breaches.
Giving preterm infants probiotics comes with relative risks so research is needed to help make this common procedure in low-risk cases, according to experts speaking at the recent International Scientific Association for Probiotics and Prebiotics (ISAPP)...
Ashwagandha suppliers are being urged to invest in defense as the UK Food Safety Agency (FSA) launches a consultation into the herb and Indian experts refute safety concerns.
The European Commission (EC) has published regulation allowing iron caseinate from milk, made by Nestlé, to be added to dietary supplements from this month (July 2024) after gaining Novel Food approval last year.
The UK’s advertising standards authority (ASA) has warned supplement firms they must remove ads which make claims to treat or cure the symptoms of menopause, as part of a wider AI-assisted campaign.
The Advertising Standard Agency (ASA) ruled that an advert for ‘Activ8 Joint Complete’ must be removed after making unauthorised health claims for bone and joint health.
Nutraceutical players are invited to give their thoughts on the implementation of of the mutual recognition regulation as part of a new consultation run by the European Commission (EC).
Described by one recent attendee as “THE microbiome research & business development event to go to in Europe”, NutraIngredients is pleased to announce the dates for Probiota 2025.
The American Herbal Pharmacopoeia (AHP) has responded to the growing number of European authorities reporting ashwagandha as an abortificient, arguing they have incorrectly cited the WHO monograph and AHP review.
The French Agency for Food, Environmental and Occupational Health & Safety (ANSES) has warned against the use of ashwagandha in a number of specific populations, making it likely operators will be advised to use label warnings.
The European Food Safety Authority (EFSA) has not been able to establish a tolerable upper intake (TUI) level for iron but has agreed a 'safe level' of 40 mg per day for adults.
A working group of 26 member states has published a report suggesting the need to ban or restrict 12 'critical' ingredients such as ashwagandha, curcumin, maca and substances like melatonin.
Despite widespread use, terms such as ‘better for you’ and ‘healthy’ can’t just be used outright. They must be used in the right context.
The European Union and the United States operate with different regulations for dietary supplements, including labeling, marketing, food additives and more. So how do brands navigate two very different regulatory environments?
As EU voters take to the ballot box this week (June 6 to 9) for the parliamentary elections, the European Federation of Associations of Health Products Manufacturers (EHPM) has called on new decision makers to pursue transparent and science-based policy.
According to one attorney, “Protein shakes, protein powders, arguably even protein bars that are advertised for muscle building” could be off limits on TikTok.
While ashwagandha investment and innovation is surging, some European authorities are showing signs of safety concern, leading industry experts to criticize a spread of "complete misinformation" across the continent.
Multiple leading medical societies from across the globe have challenged the WHO guidelines on complementary feeding for older infants and young children that recommend the introduction of cow's milk from six months of age.
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.