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Infant formulas are unique because they are the only source of nutrition for many infants during the first 4 to 6 months of life. They are critical to infant health since they must safely support growth and development during a period when the consequences on inadequate nutrition are most severe. Existing guidelines and regulations for evaluating the safety of conventional food ingredients (e.g., vitamins and minerals) added to infant formulas have worked well in the past; however they are not sufficient to address the diversity of potential new ingredients proposed by manufacturers to develop formulas that mimic the perceived and potential benefits of human milk. This book, prepared at the request of the Food and Drug Administration (FDA) and Health Canada, addresses the regulatory and research issues that are critical in assessing the safety of the addition of new ingredients to infants.
Contents
- THE NATIONAL ACADEMIES
- COMMITTEE ON THE EVALUATION OF THE ADDITION OF INGREDIENTS NEW TO INFANT FORMULA
- FOOD AND NUTRITION BOARD
- Reviewers
- Preface
- Executive Summary
- 1. Introduction and Background
- 2. Defining Safety for Infants
- 3. Comparing Infant Formulas with Human Milk
- 4. Strengthening the Current Processes to Evaluate New Ingredients for Infant Formulas
- 5. Testing Ingredients with Preclinical Studies
- 6. Going Beyond Current Clinical Studies
- 7. Selecting an In-Market Surveillance Plan
- A Acronyms and Glossary
- B Composition of Infant Formulas and Human Milk for Feeding Term Infants in the United States
- C Redbook Table of Contents
- D Applying the Recommended Approaches
- E Biographical Sketches of Committee Members
This study was supported by Contract No. 223-01-2460, TO4, and Contract No. 4500033271 between the National Academy of Sciences and the Food and Drug Administration, U.S. Department of Health and Human Services, and Health Canada. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect the view of the organizations or agencies that provided support for this project.
NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engineering, and the Institute of Medicine. The members of the committee responsible for the report were chosen for their special competences and with regard for appropriate balance.
- NLM CatalogRelated NLM Catalog Entries
- Nutrient needs and feeding of premature infants. Nutrition Committee, Canadian Paediatric Society.[CMAJ. 1995]Nutrient needs and feeding of premature infants. Nutrition Committee, Canadian Paediatric Society.. CMAJ. 1995 Jun 1; 152(11):1765-85.
- Food and Drug Administration--infant formulas; interim guidelines for nutrient composition; notice to manufacturers, packers, and distributors. Notice.[Fed Regist. 1980]Food and Drug Administration--infant formulas; interim guidelines for nutrient composition; notice to manufacturers, packers, and distributors. Notice.. Fed Regist. 1980 Mar 18; 45(54):17206-7.
- Review Evolution of infant nutrition.[Br J Nutr. 1999]Review Evolution of infant nutrition.Cuthbertson WF. Br J Nutr. 1999 May; 81(5):359-71.
- [In vitro availability of minerals in infant foods with different protein source].[Nutr Hosp. 2001][In vitro availability of minerals in infant foods with different protein source].Pérez-Llamas F, Larqué E, Marín JF, Zamora S. Nutr Hosp. 2001 Sep-Oct; 16(5):157-61.
- Review The role of dietary nucleotides in neonatal and infant nutrition.[Singapore Med J. 1998]Review The role of dietary nucleotides in neonatal and infant nutrition.Yu VY. Singapore Med J. 1998 Apr; 39(4):145-50.
- Infant FormulaInfant Formula
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