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Regulations under the Food Safety Modernization Act
and third‑party commentary say the product is “manufactured in certified facilities” and name GMP and FDA‑registered manufacturing in generic terms, but none of the available public pages or third‑par...
Foreign facilities that manufacture, process, pack, or hold dietary supplements for importation into the United States are required to register with the U.S. Food and Drug Administration (FDA) under t...
Regulatory testing to reveal multi‑generation and combined‑exposure effects of stacked‑trait genetically modified (GM) crops should treat stacks as potentially new biological entities, require molecul...