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Unredacted version of the CV shows that FDA redacted the term Aeromedical. See Clattenburg Decl. 64-65 Ex. See Clattenburg Decl. 55-58 Ex. 13. FDA also redacts articles designated as ePub ahead of print. See Id. Carome Decl. 8 Ex. A emphasis added. In this litigation pointing to a letter FDA sent Public Citizen in July 2014 FDA claims that it posts the CVs voluntarily. Clattenburg Decl. 19-21. The CVs that FDA has released contain the sorts of unlawful redactions Public Citizen challenges in...
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Any individual or organization involved in the production, distribution, or sale of food or drugs in the United States needs to comply with the regulations and guidelines set by the Food & Drug Administration (FDA).
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Food and Drug Administration (FDA) is a federal agency in the US that is responsible for protecting and promoting public health by regulating food and drug products.
Manufacturers, distributors, and importers of food and drug products are required to file with the FDA.
The FDA provides online forms and guidance on how to fill out the necessary paperwork for food and drug administration.
The purpose of food and drug administration is to ensure the safety and efficacy of food and drug products available to the public.
Information such as product ingredients, manufacturing process, safety testing, and labeling must be reported on food and drug administration forms.
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