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Food and drug administration and prescription drugs
Introduction to food tests
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The Food and Drug Administration has played an important role in the American society known today. In fact the Food and Drug Administration affects every citizen of the United States. Its main goal is to ensure knowledge of products and protection to every citizen that range from atmospheric hazards to the medicine and food consumed in the United States. A strong workforce of inspectors is responsible for monitoring trading and safety standards in the food and drug industries. Although many tasks done by the FDA go unnoticed by the average citizen, an absence of the FDA would most definitely not go unnoticed. However the importance of the FDA today is just as important as to how it got initiated. Wallace F. Jansseen, an FDA historian, in his article “The Story of the Laws Behind the Labels” writes about the initiation of the agencies that later developed into the FDA. Jansseen points out that the earliest forms of the FDA started out as the Department of Agriculture in 1862. Charles M. Wetherill was the first chemist that as a part of the Department of Agriculture. His main purpose was to test food, fertilizers, soils, and other agricultural substances. At first his experiments revolved around agricultural research but inevitably became involved in food safety to find adulterated substances. Jansseen points out that many of the substances that were tested were counterfeit, contaminated, diluted, and decomposed drugs. Eventually his practice of finding adulterated substances was noticed in 1906 as part of the Food and Drugs Act. The 1906 Food and Drugs Act, also known as the Wiley Act, was legislation that was passed as a result of efforts from Peter Collier and Dr. Harvey W. Wiley. Peter Collier was the one of the h... ... middle of paper ... ...s her claim with the help of Terri Lewis who is an FDA physical science technician. Lewis stated that all but 2.5% of the staff in her office are on furlough. Lewis is quoted “Foreign food is imported from other countries every day and with much fewer inspectors it makes the job less secure”. The FDA most definitely has the important task to assure U.S. citizens the availability of safe food and drugs. This importance was realized by the men that worked toward moving it into legislation. The resultant agency continued to enforce its policies consistently into the modern century without a loss of momentum. However if the FDA is impaired by means of a governmental shutdown then it is of great importance to continue the consistency in food and drug standards that it holds. Standards that hold great importance today like the standards of the FDA’s initiation.
... government inspection of meat products. The Pure Food and Drug act also passed after the Meat inspection Act of 1906. The packers denied the charges and opposed the bills to no avail. These bills protected the publics right to safe sanitary meat.
“Pure Food and Drug Act 1906.” 34 U.S. Stats. 768, quoted in Medicine in the Americas, Bethesda, Maryland: National Library of Medicine, 2004. http://www.ncbi.nlm.nih.gov/books/NBK22116/.
"Pure Food and Drug Act: A Muckraking Triumph." Food and Drug Act. N.p., n.d. Web. 08 Feb. 2014.
The momentum generated by the passage of the Meat Inspection Act helped secure the passage of the Pure Food and Drug Act, which had been stalled in Congress since 1905. With these two pieces of legislation, the federal government took important steps to assure the public that the food they were eating met minimu...
No Author. "Pure food and drug act." wikipedia 23 March 2005. 4 oct. 2007 .
Grabowski, Henry and John Vernon. 1986. “Longer Patents For Lower Imitation Barriers: The 1984 Drug Act”, The American Economic Review. Pages 196-198.
FDAs public health protection duties. By ensuring that products and producers meet certain standards, FDA protects consumers and enables them to know what they are
"Regulatory Information." Federal Food and Drugs Act of 1906. U.S. Food and Drug Administration, 20 May 2009. Web. 14 Apr. 2014. .
3Walker, Hugh: Market Power and Price levels in the Ethical Drug Industry; Indiana University Press, 1971, P 25.
In the beginning of the 1900’s, the country made dramatic changes toward progressivism in domestic issues. These changes were first made by President Theodore Roosevelt, who signed the Pure Foods and Drug Act of 1906. This bill was made, “For preventing the manufacture, sale, or transportation of adulterated or misbranded or poisonous or deleterious foods, drugs, medicines, and liquors, and for regulating traffic therein, and for other purposes.” This would help bring progressive change to many manufacturing industries that were newly developed in the late nineteenth century. These jobs were dangerous to an equal and fair way of living for the American working class and were resolved by this act.
1914 was a change for these drugs it was like overnight these drugs become illegal. The reason for this change in 1914 wa... ... middle of paper ... ... ment. When they modified the treatment they hinder the ability to identify the effective parts of this treatment.
The drug control policy of the United States has always been a subject of debate. From Prohibition in the early 1930’s to the current debate over the legalization of marijuana, drugs have always been near the top of the government’s agenda. Drug use affects every part of our society. It strains our economy, our healthcare, our criminal justice systems, and it endangers the futures of young people. In order to support a public health approach to drug control, the Obama administration has committed over $10 billion to drug education programs and support for expanding access to drug treatment for addicts (Office). The United States should commit more government resources to protect against illegal use of drugs by youths and provide help for recovering addicts.
The first foremost legislation in this course was the Harrison Act, approved in 1914. One of the top powerful legislative acts ever approved concerning drugs, occurred in 1914 when Congress permitted the Harrison Act (following its major sponsor, Representative Francis Burton Harrison of New York) (Harrison). The act mandated every doctor who approved substances like the opium and morphine to trace with the government officials and if some individual without such license approved these substances could be punished together with a fine and prison time. As time progressed, it was becoming more apparent that the mistreatment and harm inflicted by these ...
The history of drug use dates back to the 19th century during the US Civil War. This saw a number of policies being introduced and by the year 1898, heroine was inaccessible. The next drugs that were targeted were alcohol and by the year 1906, the US Congress passed the Pure Food and Drug Act (PFDA) to help stop the use of such drugs. The next drug that was targeted was opium and an act was passed in 1909 to ban...
...ly look at the false claims made by food industries expand on their already set regulations, making it harder for companies to get around them. However, if the FDA believes that their regulations are as specific as they can get, then there should be at least somebody to educate consumers about food labels and add more detail to nutritional value charts. Because without changing the way how information is provided and educating people, they will not be able to change their diets to improve nations overall health.