Drug Enforcement Administration

The U.S. Drug Enforcement Administration is entrusted with monitoring the war on drugs under control around the nation. DEA agents are among the top law enforcement officials in the country. The task of a DEA agent is vital because they protect our public against drug smuggling and drug abuse in the United States. Several crucial aspects of becoming a Drug Enforcement Administration agent include education, skills, and training. A profession as a DEA operator accompanies some extraordinary…

matter with my boss. It is a signed commitments with FDA given by a sponsor before or after product approved by FDA to gather additional information about a product 's safety, efficacy, or optimal use. The Food and Drug Administration Modernization Act of 1997 (FDAMA) amended the Food, Drug and Cosmetic Act signed into law on November 21, 1997 by adding a new section 506B (21 U.S.C. 356b). FDA issued a draft guidance related to this rule in April 2001. This section provides…

nonprofit organization that sets standards for dietary supplements. These standards are enforced by the Food and Drug Administration. According to the United States Pharmacopeia, Green tea extracts have been probable causes in seven cases and a possible 27 other cases of liver damage. When these supplements are taken on an empty stomach, the outcomes can be fatal (Schardt, 2012, p. 8-9). The drug glucomannan is known for reducing the amount of body fat in a person without changing their…

By the age of 70 years, smoking 30 cigarettes a day could lead to an equivalent of an extra 14 years of skin ageing. The Real Cost commercial, by the United States Food and Drug Administration, takes place at a convenient store. With the FDA creating this advertisement it shows that smoking is not just a local problem but a national one. A young teenage girl comes and tries to buy some cigarettes. However, she doesn’t have enough money so she rips of her skin to pay for them. Smoking is bad for…

This, coupled with organic chemistry (which began with the production of urea), really pushed the science towards its present form. Soon, companies like Bayer, Pfizer, and Roche turned towards research and the creation of large-scale manufacturing of drugs, which was only more propelled by the government’s desire to treat certain conditions widespread in the population and to alleviate the injuries of the world wars. Unfortunately, it wasn’t until the problem of thalidomide and adverse side…

One such agency is the FDA. This acronym stands for Food and Drug Administration. As the name implies, they deal with regulating food and drug products. Although this is not all they do. The FDA also regulates tobacco products as well, something that technically is neither a food nor drug. Agencies are assigned certain tasks and within the agencies, offices are assigned more specific tasks. The Food and Drug Administration has several of these offices. These offices include, Office of…

"Tiger" -What is TestoBoost Pro? Testoboost Pro is a testosterone booster and bodybuilding supplement. The manufacturers of Testoboost Pro claims this product will “help its customers achieve significant bodybuilding and male enhancement results through improved testosterone levels.” The pill is supposed to function by encouraging better protein synthesis and muscle development by increasing testosterone levels. The manufactor websit also claims that this product was developed over many years…

The American Medical Association (AMA) is fighting for DTC advertising to be banned. AMA states concerns people ask for drugs that are unnecessary and cost of prescription drugs is rising. According to AMA, there is “a 30% increase in money spent on ads in the past two years, which now totals $4.5 billion” (the fix, 2015). The opposing view from the pharmaceutical companies is that DTC advertising helps inform people to know what to talk to their doctor about for their health and treatment.…

Hepatopancreas cadmium concentrations Land snails are considered to serve as 'macroconcentrator' species for Cd given their exceptional ability to accumulate it in their tissues far above environmental levels (Dallinger et al., 1993). Several studies have examined the retention of dietary Cd in the soft tissues of C. aspersus under laboratory conditions, but not at exposure levels below 0.2 mg kg-1 DW (Russell, DeHaven & Botts, 1981; Laskowski & Hopkin, 1996; de Vaufleury et al., 2006). The…

took to actually get the drug on the shelf or drug become available to be picked up at a local pharmacy. There is four phase to the FDA’s Approval Process: Pre-Clinical, Clinical, NDA Review, and Post Marketing. There are steps within all the phase that need to be completed before going to the next phase until a drug is made available to the public. During the Pre-Clinical phase there are three steps that have to be completed before going to the next phase, which is the drug being developed,…