Legal/Regulatory Aspects of Herbal Products
作者： Melanie Johns Cupp
DOI: 10.1007/978-1-59259-020-9_1
关键词:
摘要: The US Food, Drug, and Cosmetic Act mandates that drugs be proven safe effective for their labeled use before marketing. This requirement does not apply to herbs, because herbal products do fall under the definition of a drug as long they are marketed prevention, diagnosis, cure, treatment, or mitigation disease. Thus, have marketing (Kurtzweil, 1999).
springer.com
sci-hub.st 参考文章(8)
Jacob S. Ziegel, A Canadian Perspective Texas Law Review. ,vol. 79, pp. 1241- ,(2001)
Charles Marwick, Growing Use of Medicinal Botanicals Forces Assessment by Drug Regulators JAMA: The Journal of the American Medical Association. ,vol. 273, pp. 607- 609 ,(1995) , 10.1001/JAMA.1995.03520320015008
A. T. Marty, The Complete German Commission E Monographs: Therapeutic Guide to Herbal Medicines JAMA: The Journal of the American Medical Association. ,vol. 281, pp. 1852- 1853 ,(1999) , 10.1001/JAMA.281.19.1852
Mark. Blumenthal, Therapeutic guide to herbal medicines (1998). pp. 685- ,(1998)
Vance Da, An ancient heritage beckons pharmacists. Wisconsin medical journal. ,vol. 96, pp. 32- ,(1997)
Clifford Goodman, F-D-C Reports National Academies Press (US). ,(1988)
M Blumenthal, WR Busse, A. Goldberg O'rourke, The Complete German Commission E Monographs ,(1999)
Rosemary R. Berardi, Handbook of Nonprescription Drugs ,(1979)