Redbook 2000: IV. A. Introduction to Guidelines for Toxicity Studies April 2007
Toxicological Principles for the Safety Assessment of Food Ingredients
Chapter IV. A. Introduction: Guidelines for Toxicity Studies
Return to Redbook 2000 table of contents
The Agency published its first set of guidelines for toxicity studies for food additives and color additives used in food in 1982 and the first revision in 1993. The guidelines presented in Chapter IV. of Redbook 2000 reflect current scientific knowledge relevant to the design, conduct, and reporting of toxicity studies used in the safety evaluation of food ingredients.
Information contained within Chapter IV.B. provides recommendations which generally apply to all types of toxicity studies and should be considered when designing toxicity studies. Chapter IV. B. currently includes: "General Guidelines for Designing and Conducting Toxicity Studies" (IV.B.1.), "Guidelines for Reporting the Results of Toxicity Studies" (IV.B. 2.), "Pathology Considerations in Toxicity Studies" (IV.B.3.), and "Statistical Considerations in Toxicity Studies" (IV.B.4.). Relevant information contained in the "General Guidelines for Designing and Conducting Toxicity Studies" (IV.B.1.) has also been incorporated into the specific studies (IV.C.3.-5.) in Redbook 2000, for your convenience.
Information presented within Chapter IV.C. of Redbook 2000 provides recommendations for the following specific types of toxicity studies:
- IV.C.1. Short-Term Tests for Genetic Toxicity
- IV.C.1.a. Bacterial Reverse Mutation Test
- IV.C.1.b. In vitro Mammalian Chromosomal Aberration Test
- IV.C.1.c. In vitro Mouse Lymphoma Thymidine Kinase Gene Mutation Assay
- IV.C.1.d. In vivo Mammalian Erythrocyte Micronucleus Test
- IV.C.3.a. Short-Term Toxicity Studies with Rodents
- IV.C.3.b. Short-Term Toxicity Studies with Non-Rodents
- IV.C.4.a. Subchronic Toxicity Studies with Rodents
- IV.C.4.b. Subchronic Toxicity Studies with Non-Rodents
- IV.C.5 One-Year Toxicity Studies with Non-Rodents
- IV.C.9.a. Guidelines for Reproduction Studies
- IV.C.9.b. Guidelines for Developmental Toxicity Studies
- IV.C.10. Neurotoxicity Studies
Other specific toxicity studies listed in the Table of Contents of Redbook 2000 will be added in the coming months. These include: acute toxicity studies and/or alternatives (Chapter IV.C.2.), carcinogenicity studies with rodents (Chapter IV.C.6.), combined chronic toxicity/carcinogenicity studies with rodents (Chapter IV.C.7.), and in utero exposure phase for addition to carcinogenicity studies (Chapter IV.C. 8.).
Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)
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