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USA FSIS Guideline for Label Approval This guideline is designed to help establishments determine whether their labels must be submitted to FSIS’ Labeling and Program Delivery Staff (LPDS) …

USA New Directory of Ingredients Used in Products Marketed as Dietary Supplements The U.S. Food and Drug Administration (FDA) has updated the agency’s Ingredient Directory, including renamin…

USA FDA announces availability of Additional Submission Tools for Cosmetic Facility Registration and Product Listing The U.S. Food and Drug Administration (FDA) officially launched additiona…

USA Structured Product Labeling (SPL) Implementation Guide with Validation Procedures for Cosmetic Product Facility Registrations and Product Listings The U.S. Food and Drug Administration p…

USA Canada Three New Food Enzymes Granted Approvals On October 11, 2023, Health Canada unveiled NOM/ADM-0209 with immediate effect, modifying the List of Permitted Food Enzymes to enable …

USA FDA Issues Draft Guidance on Registration and Listing of Cosmetic Product Facilities and Products FDA is seeking comments on its newly developed draft electronic submission portal (Cosme…