Marguerite Klein, MS, RD
Sample Reading Materials

Department of Health and Human Services, US Food and Drug Administration. Current good manufacturing practice in manufacturing, packaging, labeling, or holding operations for dietary supplements; final rule. Petition to request an exemption from 100 percent identity testing of dietary ingredients; interim final rule. Federal Register. June 25, 2007; 72(121):34751-34958.
(Text Version Pages 34752-34800 | Pages 34801-34850 | Pages 34851-34900 | Pages 34901-34950 | Pages 34951-34958)

US Food and Drug Administration. Guidance for Industry: Botanical Drug Products. June 2004. 52 pages.
(Text Version)