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Drug laws development

U.S. Laws and Regulations Related to Drug Product Development and Manufacture. Until early in the twentieth century, dmg products were made and sold in the United States having virtually no imposed control. QuaUty was generally poor. Many products were patent medicines of dubious value. Some were harmful and addicting. [Pg.225]

C. Peck, Drug development improving the process, Food Drug Law J., 52 (1997). [Pg.825]

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]

A resource to help state legislatures develop programs for their own states that reports on trends in prescription drug laws (and many other topics) among the 50 states. [Pg.213]

Milne, C., K. Kaitin, and E. Ronchi. 2004. Orphan Drug Laws in Europe and the US Incentives for the Research and Development of Medicines for Diseases of Poverty. WHO Commission on Macroeconomics and Health, CMH Working Paper Series, Paper No.WG2 9. Available at http //www.cmhealth.org/docs/wg2 paper9.pdf [Accessed May 10, 2005]. [Pg.55]

As part of its support for the legalization of medical marijuana, NORML advocates the complete decriminalization of marijuana, a step that would remove all penalties for the private possession and the responsible use of marijuana by adults. Under this scenario, private marijuana users, including those with serious medical conditions, would not be arrested, but large-scale commercial sellers would still be violating drug laws. NORML also calls for the development of a legally controlled market for marijuana in which adult consumers could buy marijuana for personal use from safe, legal sources. [Pg.92]

With the coincidental retirement in 1962 of Commissioner Anslinger and the Supreme Court s decision that addiction was a disease, and with the arrival of President Kennedy s New Frontier, the Bureau s approach was becoming anachronistic. The prevailing mood of the day encouraged reduced penalties, more medical treatment, possible development of maintenance clinics, and a reevaluation of drug laws. In 1962 a White House Panel on Narcotic and Drug Abuse reported that It is the opinion of the Panel that the hazards of marijuana per se have been exaggerated and... [Pg.363]

Drug Use in the United States 27 Medical Science and Drug Use 32 Development of Drug Laws 32 The San Francisco Ordinance 33 Pure Food and Drug Act 33 Harrison Narcotics Tax Act 33 Alcohol Prohibition 35 Post-Prohibition Legislation 36 Current Drug Laws 37 Summary 41... [Pg.7]

Despite the principle of informed consent, ethical difficulties in human research remain. After all, when a new drug is developed, someone has to be the first person to take it. Even though federal law says that a drug must be tested extensively in animals before it is tried with people, some side effect not detected in the animal studies could still occur. [Pg.121]

It has been said that the drug law in the United States developed in the eighteenth and nineteenth century with all the red, white and blue of the anilene dyes that quickly became available. Regulations in this country rapidly developed in a characteristically idiosyncratic manner. [Pg.396]

Garbutt BJ, Hofmann ME. 2003. Recent developments in pharmaceutical products liability law failure to warn, the learned intermediary defense, and other issues in the new millennium . Food Drug Law J. 58(2) 269-286. [Pg.616]

Palumbo FB, Mullins CD. 2002. The development of direct-to-consumer prescription drug advertising regulation. Food Drug Law J. 57 423-443. [Pg.664]


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See also in sourсe #XX -- [ Pg.32 ]




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