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anon, Guidance for Industry: Container Closure Systems for Packaging Human Drugs and Biologics, May 1999, Food and Drug Administration, Center for Drug Evaluation and Research, Lockhart, H., and Paine, F.A., "Packaging of Pharmaceuticals and Healthcare Products", 2006, Blackie, ISBN 0-7514-0167-6
Food packaging is a packaging system specifically designed for food and represents ... Some are country specific such as the US Food and Drug Administration and the ...
Fair Packaging and Labeling Act (US) FDA Food Safety Modernization Act; Federal Food, Drug, and Cosmetic Act; Federal Meat Inspection Act; Food and Drug Administration Amendments Act of 2007; Food and Drug Administration Modernization Act of 1997; Food libel laws; Food Quality Protection Act; Generally recognized as safe; Global Food Security ...
Food additives, the U.S. Food and Drug Administration (FDA) explains, are “any substance the intended use of which results or may reasonably be expected to result, directly or indirectly, in its ...
The additives that Trasande is worried about include phthalates (used in personal care products and food packaging), bisphenols (used in aluminum can linings and thermal paper receipts) and per ...
The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics.
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