Comprehensive Drug Prevention And Control Act Of 1970 Essay

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Gabrielle Wheat Jan 2012 SOS-304-GS WA2 1. (a) Describe the essence of the process by which a pharmaceutical company and the Food and Drug Administration (FDA) function in the development of a new medication, showing understanding of conflicts of interest that sometimes occur. (b) Describe the Comprehensive Drug Abuse Prevention and Control Act of 1970. Include the criteria for listing a drug as a Schedule 1 – Schedule V controlled substance and give some examples of drugs that are in the Schedule 1 – Schedule V. (c) Describe the major elements of recent federal approaches to the enforcement of our drug laws, and indicate some of the enormous difficulties and apparently positive consequences associated with those approaches. 1A. The Food and Drug Administration (FDA) monitor drugs that have been altered and ones that did not correctly list certain ingredients. The FDA also looks into drugs that are considered to be therapeutic. When the FDA first came about many companies found loop holes that the FDA did not approve of. For example in 1922 the FDA went after the B&M External Remedy. Its manufacturers truly believed it was a cure for tuberculosis. This made a loop hole that made it seem like anyone who…show more content…
The Comprehensive Drug Abuse Prevention and Control Act of 1970 came into law because of the simple fact that there were so many other regulations that were making things very confusing. By 1970 there were a lot of laws on the enforcement of drug use and sales. These laws had modifications and amendments. Another reason for The Comprehensive Drug Abuse Prevention and Control Act of 1970 was because of the punishments that people got for breaking these drug use and sale laws. The death penalty was among some of these rigid penalties one could receive. The Comprehensive Drug Abuse Prevention and Control Act of 1970 started off with a “clean slate” that was established off of the new facts and research that had been done on
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