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Food and drug law

Tennessee s Department of Agriculture prohibits the use of DDT because its Food and Drug Law considers a food adulterated if it may have become contaminated. This is possible, it is alleged, when DDT is used. Knoxville s Health Bureau, on the other hand, permits the use of residual sprays, provided the food is protected from contamination, and the food must be pure and wholesome. ... [Pg.27]

Food and Drug Laws that Affect Drug Product Design, Manufacture, and Distribution... [Pg.627]

Chemistry, U.S. Department of Agriculture, began investigating food and drug adulteration the following year he recommended enactment of a national food and drug law... [Pg.627]

Milestones in U.S. Food and Drug Law History, Publ. (FDA) 73-1018, U.S. Dept, of Health, Education, and Welfare, Food and Drug Administration, Washington, DC, 1972. [Pg.642]

FDLI. (1999). Compilation of Food and Drug Laws, Vol I II, Food and Drug Law Institute, Washington. [Pg.97]

Pilot, L. and Waldemann, D. (1998). Food and Drug Modernization Act of 1997 Medical device provisions. Food and Drug Law J. 53 267-295. [Pg.98]

Pendergast, W. (1984). Biological drug regulation. In The Seventy-fifth Anniversary Commemorative Volume of Food and Drug Law. Edited and Published by the Food and Drug Law Institute, Washington, D.C., pp. 293-305. [Pg.174]

The growth of technology has, therefore, led to branches of law which are in their early stages of development. Environmental protection law, food and drug law, consumer protection law, and others are opportunities available to the lawyer trained in chemistry or chemical engineering. [Pg.11]

Chief chemist Peter Collier recommends a national food and drug law during the next 25 years, more than 100 such biUs are introduced. [Pg.494]

Source From Milestones in U.S. Food and Drug Law History, www.fda.gov/opacom/backgrounders/miles.html... [Pg.495]

Hutt PB. A historical introduction. Food Drug Cosmetic Law J 1990 45 17 The transformation of United States Food and Drug Law. / Association... [Pg.598]

Peter Barton Hutt, Senior Coimsel Covington and Burhng, Washington DC USA Lecturer in Food and Drug Law, Harvard Law School, Cambridge MASS Former Chief Counsel to the US Food and Drug Administration (FDA)... [Pg.876]

CUssold, D. B. 1995. Prescription for The Orphan Drug-Act The Impact of the FDA s 1992 Regulations and the Latest Congressional Proposals for Reform. Food and Drug Law Journal 50(1) 125-147. [Pg.296]

Pines, Wayne L. 1999. A History and Perspective on Direct-to-Consumer Promotion. Food and Drug Law Journal 54 489-518. [Pg.311]

Siegel, Jonathan B. 2004. Financial Aspects of 180-Day Generic Exclusivity. Presentation to the Food and Drug Law Institute Conference on Two Decades of Hatch-Waxman, December 1-2, Washington, DC. [Pg.313]


See other pages where Food and drug law is mentioned: [Pg.23]    [Pg.2]    [Pg.4]    [Pg.23]    [Pg.627]    [Pg.627]    [Pg.628]    [Pg.104]    [Pg.113]    [Pg.325]    [Pg.326]    [Pg.288]    [Pg.38]    [Pg.36]    [Pg.50]    [Pg.59]    [Pg.972]    [Pg.57]    [Pg.130]    [Pg.130]    [Pg.131]    [Pg.139]    [Pg.140]    [Pg.8]    [Pg.494]    [Pg.238]    [Pg.274]    [Pg.602]    [Pg.20]    [Pg.72]    [Pg.83]   
See also in sourсe #XX -- [ Pg.328 ]

See also in sourсe #XX -- [ Pg.2841 ]




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