Regulatory

Conference in India geared to help New Delhi-based decision makers.

Tate & Lyle’s soluble corn fiber product is the latest in a list of approvals.

KLEAN-D vitamin D supplement is the seventh supplement in the product range deemed free of banned substances.

The antioxidant can now be used in low fat meat, poultry and fish products.

Panel also issues dosage recommendations.

The legal U.S. limit for gluten in a "gluten-free" product is now 20 parts per million.

Earlier this week, NPA and AHPA announced support for various GMO labeling schemes.

Alpha-cyclodextrin is often used in the food industry as a water-soluble dietary fiber, in products such as dairy, bakery, muesli bars, and breakfast cereals.

MegaFood’s Blood Builder, Wild Blueberry, Magnesium, Calcium, and Calcium Magnesium and Potassium supplements are now certified non-GMO.

EFSA responds to a health claim application from collagen protein firm Gelita.

The health claims apply to Cereboost when included at a 200 mg daily dose.

Sunfiber can help lower postprandial glucose levels by more than 20%.

Has FDA effectively slammed the door shut on DMAA?

The National Organic Standards Board is prohibiting nonorganic annatto extract, while welcoming algae as a new source of beta-carotene extract.

The U.S. Department of Commerce determines final dumping margins for Chinese and Austrian producers of xanthan gum.

Which provides the better regulatory pathway?

A New York senator proposes a new bill targeting the sports performance market.

Labeling caffeine content is a job for all industry members.

Five dietary supplement associations sent new comments to FDA recently regarding the agency’s new dietary ingredient (NDI) draft guidance and NDI ingredient identity.

The Israel-based private-label confectionery manufacturer selected ingredients that meet EFSA weight management claims or that are clinically proven: glucomannan and potato-derived ingredient Slendesta.

Why your NAD challenges will build a stronger marketplace for dietary supplements.

A Superior Court judge rules in favor of a group of dietary supplement companies in a Prop 65 case.

While the guidelines are not mandatory for CRN members, they are recommended.

The GAO reports that FDA increased its number of AER inspections from 120 in 2008 to 410 during the period spanning January–September 2012.

Monk fruit extract will now be added to Canada’s List of Permitted Sweeteners.

Thanks to the efforts of one industry firm, self-affirmed GRAS records are now compiled in one, collective database.

Crucial transition periods related to Canada’s Natural Health Products Regulation.