New Jersey-based contract manufacturer Vitaquest International received food safety standards certification by global certifying body DNV GL Business Assurance.
The latest intensification of the US China trade war will compress margins and could constrict supply, experts in the import of dietary ingredients have said.
A new water dispersible curcumin ingredient using a water dispersible technology has hit the US and European markets, courtesy of the new DolCas-Tenshi partnership. The pairing is also bringing a men’s sexual heath ingredient to market.
Neptune Wellness Solutions has completed a radical refocus of the company with the announcement of its entry into the hemp/CBD market in the United States.
The hemp/CBD industry is being threatened by so-called synthetic cannabinoids that are flooding the market, attendees at a recent botanicals conference were told.
The recent slew of crackdowns, regulatory reviews and stricter rules for China's health food and supplement industry are 'growing pains' the industry must overcome, as regulators double down on efforts to promote safety and collect taxes.
Steering a course toward rigorous supply chain integrity will help dietary supplement manufacturers navigate an increasingly turbulent market churned by commoditization.
Unlike pharmaceuticals, the effects of nutritional supplements are subtle. We spoke with several contract research organizations that specialize in human clinical trials for nutritional interventions to learn how companies can validate liver health claims.
China’s State Administration for Market Regulation (SAMR) and the Ministry of Commerce summoned all 91 direct-selling firms operating in China to a meeting as part of the “100-day operation” to clean up the health food market.
Ninety-eight per cent of the approved health food filings in China over the last 18 months went to domestic firms, a Chinese regulatory consultancy has found.
The Natural Products Association has objected to a proposal by the US Food and Drug Administration that NPA says will result in an expanded sharing of information on US firms with foreign governments. NPA said the proposal lacks transparency and runs...
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.
