Should Changes Be Made To The Food And Drug Administration?

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Should changes be made to the Food and Drug Administration? Over the years, we have heard about countless circumstances where products that have been approved by the FDA have caused severe health problems and even death. These products range from prescription medications to the use of approved medical devices. The Food and Drug Administration (FDA) responsibilities include ensuring the safety and security of our nation's food supply, dietary supplements, tobacco products, cosmetics, veterinary products, prescription and over-the-counter medications, as well as, a variety of other medical products. In addition, the FDA is responsible for approving innovations that are proven to be safe, effective, and affordable in improving and maintaining the overall health of the public. (FDA, 2013) Due the researcher's own interests in the public's health and well-being, the primary goal for this project is to determine any issues regarding the monitoring and regulations of products approved by the FDA for public use.
The major sections of the paper will include: * Current regulations * Recent outcomes from the use of specific FDA approved products * Areas that need improvement in the regulation process will be identified
In gathering information regarding the specified topic, research will be conducted to clearly answer who the FDA is and the specific purpose of the administration. What procedures are used before approving a product? What steps are taken if a marketed product is determined to be unsafe? When is the public notified of recalled products? How does the administration address the issues?
The research plan consists of gathering information from resources available on

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