Nobody downloaded yet

FDA policy - Essay Example

Comments (0) Cite this document
Name Instructor Course Date FDA Policy Introduction The Food and Drug Administration is an agency in the US Department of Health and Human Services. It tests, observes, endorses, and sets up safety standards for chemicals, foods and food additives, cosmetics, drugs, medical and household devices…
Download full paperFile format: .doc, available for editing
GRAB THE BEST PAPER94.4% of users find it useful
FDA policy
Read TextPreview

Extract of sample
"FDA policy"

Download file to see previous pages FDA policies regarding raising chicken FDA defines precisely how chicken should be raised in terms of the treatment given and the methods used to keep them. Its policies outline how antibiotics should be used or should not be used in poultry production. This is to slow down the development of bacteria that are resistant to antibiotics. The agency has trumpeted the policies as the beginning of termination of the misuse of drugs on chicken (Allport-Settle 30). However, the FDA missed the point. While the policies call for the end of using antibiotics to make chicken grow faster, they approve continuous use of such drugs to compensate for unsanitary and overcrowded conditions and prevent diseases at firm operations that produce poultry food. The prophylactic or preventive use of antibiotics resembles their use for growth promotion including similar low doses that are equally responsible in the antibiotic resistance. The FDA encourages the use of preventive drugs necessary to assure chicken health. Left unaddressed is whatever that makes this use ‘necessary’. The use of antibiotics to make chicken grow faster seems to be in its last stages, though much will depend on how rapidly drug companies comply with the policies and whether the food poultry industry complies at all. According to the public health advocates, the fight now shifts to the use of such drugs to prevent diseases. This is a much steeper hill to scale; their misuse lies at the center of industrial food poultry production, yet the FDA has renounced its responsibility to stop it. In 2005, FDA banned the use of fluoroquinolone in poultry production in the US to reduce the occurrence of fluoroquinolone-resistant Campylobacter. However, little is known regarding the potential effectiveness of this policy (Luangtongkum 72). A research was conducted with an objective of following temporal changes in the occurrences of Campylobacter among chicken from two conservative producers who declared their termination of fluoroquinolone use in 2002, only three years before the FDA’s ban. Another objective was the occurrence of this antibiotic disease in conventional chicken products to those from producers who do not use antibiotics. Chicken samples were collected from three antibiotic-free keepers and two conventional chicken keepers over the course of five months in 2004 and 15 weeks in 2006. Fluoroquinolone resistance rates were compared among Campylobacter isolates from the diverse producers. From the results, it was established that there was no major change in the percentage of fluoroquinolone-resistant Campylobacter segregates from the two conventional keepers over the period of study. Further, Campylobacter strains from both producers were significantly more probable to resist fluoroquinolone compared to those from the antibiotic-free ones. Therefore, fluoroquinolone-resistant Campylobacter might be persistent contaminants of chicken products even after ceasing to use on-farm fluoroquinolone. The FDA’s ban on the use of this antibiotic in chicken rising may therefore be insufficient in reducing resistant Campylobacter in chicken products. FDA policies regarding genetically engineering corn For about two decades, FDA has been analyzing genetic modification methods for drug-biological growth as well as the development of new foodstuffs. The agency has carefully created policies to accommodate the evolving and changing world of biotechnology. ...Download file to see next pagesRead More
Cite this document
  • APA
  • MLA
(“FDA policy Essay Example | Topics and Well Written Essays - 1250 words”, n.d.)
Retrieved from
(FDA Policy Essay Example | Topics and Well Written Essays - 1250 Words)
“FDA Policy Essay Example | Topics and Well Written Essays - 1250 Words”, n.d.
  • Cited: 0 times
Comments (0)
Click to create a comment or rate a document
FDA Regulation of Tobacco Products in the United States
Although some drugs are meant to cure illnesses, when taken in overdose, these result in negative effects. Similarly, other drugs, which are illegal, such as marijuana, are harmful to human health. Tobacco is equally harmful, although it is not a drug in itself, but rather, a carrier of nicotine, which is highly addictive.
7 Pages(1750 words)Essay
Federal Drug Policy Paper
The strategy under discussion in this paper shows several areas of weakness. The strategy increases educational resources for drug testing programs in schools, and its media campaign expands advertising and public communication outreach intended to change teen beliefs and intentions toward drug use.
3 Pages(750 words)Essay
An Investigation Of Food Labelling
While calories, trans fats, and nutrition can guide us to a healthy lifestyle, allergens can be life-threatening. This concern is especially relevant to restaurants that have the responsibility to monitor their food's ingredients. The US FDA has identified a list of allergens that they require be labelled with plain language.
4 Pages(1000 words)Essay
Biologic Manufacturing and the FDA
As part of the agreement, a dividing scheme was laid out, which has been criticized for its complexity and lack of consistency. For example, human-tissue derived products are classified as drugs, but human blood-derived products are classified as biologics.
2 Pages(500 words)Essay
Prescription Health Care Costs and its Effects on the Elderly
tion drugs have significant health benefits as they alleviate the need for surgery and other invasive treatments ad thus hasten the recovery process especially among the elderly (Shang & Goldman, 2007). In most cases newer drugs which have relatively less side effects are
5 Pages(1250 words)Essay
MPH522 - Public Health Law and Policy, Mod 3 Case Assignment
There are those, however, that are in fact building new public health law with the CDC being one of those (Fox, 2001). This paper will discuss the case review of Nutritional Health Alliance vs. Food and Drug
3 Pages(750 words)Essay
Through my professional journey, I have recognized that there are enumerable health concerns and issues in the area of public health that need to be addressed. It is this drive
2 Pages(500 words)Essay
Public Policy
The control and use of Marijuana had gone out of hand, forcing the federal government through a congress agreement, to develop acts that could minimize its use. This
2 Pages(500 words)Essay
Evaluating the Effects of Regulatory Agencies on the LIMS ( Laboratory Information Management System )
By integrity, both regulatory agencies will expect that the truth of the medical data, both in terms of patient records and general pharmaceutical
7 Pages(1750 words)Essay
Policy formation
The problems within the scope of American healthcare, therefore, have affected the nation’s politics as many leaders focus on the issues and proper implementation of policies meant to curb the
3 Pages(750 words)Essay
sponsored ads
We use cookies to create the best experience for you. Keep on browsing if you are OK with that, or find out how to manage cookies.
Let us find you another Essay on topic FDA policy for FREE!
Contact us:
Contact Us Now
FREE Mobile Apps:
  • About StudentShare
  • Testimonials
  • FAQ
  • Blog
  • Free Essays
  • New Essays
  • Essays
  • Miscellaneous
  • The Newest Essay Topics
  • Index samples by all dates
Join us:
Contact Us