The Secretary of Health and Human Services has the authority to issue regulations outlining what constitutes good manufacturing practice for dietary supplements, per section 402(g) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.…
U.S.A
The FDA has decided to reopen the comment period for the draft guidance titled "Labeling of Plant-Based Milk Alternatives and Voluntary Nutrient Statements; Draft Guidance for Industry" that was published on February 23, 2023, in the Federal…
The FDA issued a Request For Information to gather feedback from stakeholders about food labeling information provided through online grocery shopping platforms, as part of the Biden-Harris Administration’s National Strategy on Hunger, Nutrition…
FDA explains in answer to those inquiries that there is no price associated with registering a food facility with FDA and that registrants are not obliged to engage a third-party company or "registrar" to register their facilities with FDA.
Perfluoroalkyl and polyfluoroalkyl substances (PFAS) is an abbreviation for a wide category of synthetic organic compounds.
The U.S.
The Food and Drug Administration (FDA) has released a guidance document in the shape of frequently asked questions (FAQs) to cater to Medical Food Manufacturers. ||
Activities for the Safety of Imported Seafood was published by the FDA. The report details the FDA's all-encompassing strategy for guaranteeing that U.S.
Colorado is the most recent state to propose legislation aimed at limiting access to weight management products, following similar initiatives in Maryland, California, New York, and other places.
Two bills were reintroduced on March 17, 2023, in the U.S. House that would compel the Food and Drug Administration to regulate cannabidiol (CBD) produced from hemp.