Code of Federal Regulations 40 CFR Part

U S Code of Federal Regulations 21 CFR Part 314 21 CFR Part 514 21 CFR Part 601 U S Food, Drug Cosmetic Act Chapter 5, Sub chapter B, F... 

Computer System Validation US Code of Federal Regulations 21 CFR Part 11. 

Title 21 Code of Federal Regulations (21 CFR Part 11), Electronic Records Electronic Signatures, FDA, 2003 (http //www.fda.gov). Validation/compliance documents found under the Parenteral Drug Association (PDA) (http //www.pda.org). 

FDA-certifiable color additives are batch certified by the United States Food and Drug Administration using analytical chemistry methods developed for this purpose by the FDA. The color additive regulations are described in Title 21, Parts 70 to 82, of the United States Code of Federal Regulations (21 CFR Parts 70 to 82). The batch certification process is described in 21 CFR Part 80. Current certification analytical methods are available from the Office of Cosmetics and Colors, Colors Certification Branch (HFS-107), U.S. Food and Drug Administration, 5100 Paint Branch Parkway, College Park, Maryland 20740. 

Food and Drug Administration. 2001. Code of Federal Regulations (21 CFR), Parts 11, 50, 54, 56, 312, 314, 1st edition. Brookwood Medical Publications. 

Anon (2000b) Title 21 code of federal regulations (21 CFR part 58). Good laboratory practice for nonclinical laboratory studies... 

In the United States (US) framework, regulations published by the Food and Drug Administration (FDA) concerning cosmetic products can be found in Title 21 of the Code of Federal Regulations (21 CFR) Parts 700-740, which states that ( ) ingredient means any single chemical entity or mixture used as a component in the manufacture of a cosmetic product . 

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