On March 6, 2023, the Food and Drug Administration (FDA) launched a new directory of ingredients used in dietary supplements. The directory will be a “one-stop shop” for ingredient information […] Read More >>
On December 20, 2022, the Federal Trade Commission (FTC) published “Health Products Compliance Guidance” for advertising and marketing health claims. The guidance document replaces “Dietary Supplements: An Advertising Guide for […] Read More >>
On Thursday, November 17, 2022, the Center for Food Safety and Applied Nutrition issued seven warning letters to manufacturers of supplements marketed for the promotion of cardiovascular health. The dietary […] Read More >>
The FDA recently published responses to several new dietary ingredient notifications (NDIN) submitted for nicotinamide mononucleotide (most notably the November 8, 2022 response to Inner Mongolia Kingdomway Pharmaceutical Ltd. “Kingdomway”). […] Read More >>
To be used in foods and dietary supplements, ingredients must: be determined to be Generally Recognized as Safe (GRAS), be approved as a New Dietary Ingredient (NDI), be considered an […] Read More >>
Just months after announcing that new documentation would be required for supplements sold on their marketplace, Amazon has again updated their requirements, this time without an announcement. In this latest […] Read More >>
Are you concerned that the dietary products that you consume are safe and that the environment in which they are manufactured is up to a particular standard? Well, you should […] Read More >>
Dietary supplement marketers selling on Amazon are now being asked to provide testing results and other manufacturing information on their supplement products in order to remain on Amazon’s site for […] Read More >>
On February 11, 2019, FDA Commissioner Dr. Scott Gottlieb announced that the regulatory framework for dietary supplements is expected to change. It has been determined that changes are necessary due […] Read More >>
Prop 65, California’s right-to-know law that requires a clear and reasonable warning for chemicals known to cause cancer or reproductive harm, finds that coffee does not require a cancer warning. […] Read More >>
The Food Safety Modernization Act (FSMA) reaches across the entire food industry, not just conventional foods. Stakeholders and consumers rarely think of dietary supplements as foods, even though they are […] Read More >>
January 2017 FDA has released a guide to aid industry comply with the new nutritional labeling requirements as per the final rule. Service(s) Related to Post: Nutritional Labeling Following the […] Read More >>
dicentra will be participating in various trade show exhibitions and conferences throughout this year. Get the chance to meet us at our booth at the following upcoming 2016 shows: GFTC […] Read More >>
Sign Up for GMP Online Training Now! Companies that manufacture, package, label, or import dietary supplements or health products for sale in Canada and the U.S. must ensure that their […] Read More >>
Health Canada’s Non-Prescription Drug Monograph Attestation Pilot has just ended, low success rate will result in revisions to the process. Health Canada initiated a Non-prescription drug monograph attestation pilot in […] Read More >>
If you know what Temporary Market Authorization (TMA) means and your company sells Caffeinated Energy Drinks in Canada, get ready to be puzzled. Maybe grab an energy drink to fuel […] Read More >>
USDA’s Process Verified Program verifies facility process of manufacture can ensure products do not contain GMO ingredients. This ground-breaking distinction was achieved by SunOpta’s food manufacturing facility in Hope, […] Read More >>
FDA releases draft guidance for Voluntary Qualified Importer Program to provide better market access for compliant Importers. Are you aware that on June 6, FDA began asking for comments […] Read More >>
Three final guidance documents and one draft guidance were recently released on FDA nanomaterials regarding the development of nanotechnology in food, dietary supplements, and cosmetic products and reflects FDA’s current […] Read More >>
In June 2014, the FDA has announced the release of the final compliance policy guide for food facility registration entitled “Compliance Policy Guide Sec. 100.250 Food Facility Registration – Human […] Read More >>
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