The source of CBD should be of concern for the companies marketing the ingredient, said a legal expert at a recent dietary supplement industry event. But he also said the regulatory landscape for the ingredient is shifting so fast that any opinions he...
As the Supplement OWL approaches 12,000 labels in its Tier 1 product label library, the Council for Responsible has announced a new pilot program to build out Tier 2, which will be known as the Commercial Data Exchange, or CDX.
A new guidance from FDA on how to determine facility status under FSMA is a step forward in applying these rules to the dietary supplement industry, an expert says.
Supplement critic Dr Pieter Cohen has trained his sights on probiotics for a new opinion paper, stating that the sector has spun hundreds of small studies favorably and also practices creative advertising.
The latest Botanical Adulterants Bulletin focuses on the increasing popular botanical ingredient: maca (Lepidium meyenii, syn. L. peruvianum, Brassicaceae) root and root extract.
Analysis of 35 commercial dietary supplements of Goldenseal (Hydrastis canadensis L.) showed that only three did not contain what they claimed to contain. Goldenseal adulteration is well documented, and one expert says it's difficult to believe that...
A recent USP stakeholder meeting wrestled with the thorny issue of how to put some kind of standards around the use of DNA techniques for botanical ingredient identification. The word from one of the attendees is that it is far too early to tell where...
Natreon has announced an organic certification on its PrimaVie shilajit ingredient. As this is not an agricultural commodity, the company views the certification as more of a statement of overall quality rather than primarily a verification of its production...
Instead of relying on a ‘precautionary zero tolerance’ for pesticide residue in dietary supplements, NSF International updated the maximum allowable level for companies to pass its quality test.
NutraChampion winner Judy Blatman said she has seen a maturation of the dietary supplement industry in her time at the Council for Responsible Nutrition and sees great potential for the future.
The Food and Drug Administration (FDA) is soliciting comments for a GMP code in which ingredient companies can petition for skip lot testing, but one trade group found discrepancies in the Federal Registrar notice.
From profiling their ingredient suppliers to setting up codes consumers can look up, supplement brands are using transparency to win over consumer trust.
The Florida Department of Agriculture and Consumer Services (FDACS) now requires saw palmetto harvesters and sellers to obtain a special permit, winning applause from ingredient suppliers and botanical industry trade groups.
