Regulatory Agency In Health Care

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Regulatory Agency Paper May 30, 2012 University of Phoenix Axia Online Introduction: A regulatory agency is a department or division of a government entity, and is focused on setting and enforcing the standards dictated by law in regard to trade issues. In the following assignment, a governmental/regulatory agency that governs/regulates the health care industry or a particular segment of the industry will be identified, then will follow a description of the history of the agency, the source and scope of its authority, its structure, how it carries out its day-to-day responsibilities, and its effects on the health care industry or a particular segment of the industry. Furthermore, the federal government holds the responsibility to ensure…show more content…
S. federal government. Its origins go all the way back to the appointment of Lewis Caleb Beck in the Patent Office in 1848 to carry out chemical analyses of agricultural products, a function that the newly created Department of Agriculture inherited in 1862. Although it was not known by its present name until 1930, FDA’s modern regulatory functions began with the passage of the 1906 Pure Food and Drugs Act, a law a quarter-century in the making that prohibited interstate commerce in adulterated and misbranded food and…show more content…
Therefore, doctors, physician assistants, nurses, pharmacists, and the individual themselves are in fact what makes up the the health care industry that needs to reduce the risks from using medicines and to get the most benefit out of them. In order to make medicine use safer, one must speak up about their past and present because the more information a health care organization knows about them, the better they can plan the care that’s right for them. Another important factor that FDA effects in the health care industry is finding the correct facts. Before the health care organization can decide on a prescription or OTC medicine, one must know understand as much about it as possible. The most important factors to identify are brand and generic names, active ingredients, inactive ingredients, uses, warnings, possible interactions, side effects, possible tolerance, dependence, or addiction, overdose, directions, storage instructions, and expiration

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