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Guidance for applicants on health claims |
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Guidance for Industry: Frequently Asked Questions About GRAS |
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Guidance for Industry: Enzyme Preparations: Recommendations for Submission of Chemical and Technological Data for Food Additive Petitions and GRAS Notices |
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Guidance for Industry: Enzyme Preparations: Recommendations for Submission of Chemical and Technological Data for Food Additive Petitions and GRAS Notices |
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Guidance for Industry: Estimating Dietary Intake of Substances in Food |
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Guidance for Industry: Recommendations for Submission of Chemical and Technological Data for Direct Food Additive Petitions |
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Guidance for Industry: Summary Table of Recommended Toxicological Testing for Additives Used in Food |
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Guidance for Industry: Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements |
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Guidance for Industry: Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements |
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Guidance for Industry: Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements |
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Guidance for Industry: Assessing the Effects of Significant Manufacturing Process Changes, Including Emerging Technologies, on the Safety and Regulatory Status of Food Ingredients and Food Contact Substances, Including Food Ingredients that Are Color Additives |
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GUIDANCE ON THE IMPLEMENTATION OF REGULATION N° 1924/2006 ON NUTRITION AND HEALTH CLAIMS MADE ON FOODS CONCLUSIONS OF THE STANDING OMMITTEE ON THE FOOD CHAIN AND ANIMAL HEALTH |
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ADMINISTRATIVE GUIDANCE ON SUBMISSIONS FOR SAFETY EVALUATION OF SUBSTANCES ADDED FOR SPECIFIC NUTRITIONAL PURPOSES IN THE ANUFACTURE OF FOODS |
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GRAS Regulatory Submissions |
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Draft Guidance for Industry: Exempt Infant Formula Production: Current Good Manufacturing Practices (CGMPs), Quality Control Procedures, Conduct of Audits, and Records and Reports February 2014 |
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Guidance for Industry: Frequently Asked Questions about FDA's Regulation of Infant Formula March 1, 2006 |
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Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related IssuesJuly 2011 |
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Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related IssuesJuly 2011 |
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Liquid Dietary Supplements: Guidance for Industry: Distinguishing Liquid Dietary Supplements from Beverages January 2014 |
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Liquid Dietary Supplements: Guidance for Industry: Distinguishing Liquid Dietary Supplements from Beverages January 2014 |
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Substances added to Foods and Beverages: Guidance for Industry: Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements January 2014 |
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Substances added to Foods and Beverages: Guidance for Industry: Considerations Regarding Substances Added to Foods, Including Beverages and Dietary Supplements January 2014 |
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Liquid Dietary Supplements: Draft Guidance for Industry: Factors that Distinguish Liquid Dietary Supplements from Beverages, Considerations Regarding Novel Ingredients, and Labeling for Beverages and Other Conventional Foods (December 2009) |
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Liquid Dietary Supplements: Draft Guidance for Industry: Factors that Distinguish Liquid Dietary Supplements from Beverages, Considerations Regarding Novel Ingredients, and Labeling for Beverages and Other Conventional Foods (December 2009) |
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Frequently Asked Questions about FDA's Regulation of Infant Formula |
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Frequently Asked Questions about FDA's Regulation of Infant Formula |
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Guidance for health claims related to gut and immune function |
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Guidance on health claims related to antioxidants, oxidative damage and cardiovascular health |
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Guidance on the scientific requirements for health claims related to appetite ratings, weight management, and blood glucose concentrations |
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Guidance on the scientific requirements for health claims related to bone, joints, skin and oral health |
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Guidance on the scientific requirements for health claims related to physical performance |
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Guidance on the scientific requirements for health claims related to functions of the nervous system, including psychological functions |
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Guidance for Industry: Demonstration of the Quality Factor Requirements Under 21 CFR 106.96(i) for "Eligible" Infant Formulas June 2014 |
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