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Pros And Cons Of Food And Drug Administration

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In the United States and many other countries, the government allots a certain amount of money to go into different public institutions. A public institution is an institution that is run by and funded by the government. One example of a public institution would be the Food and Drug Administration otherwise known as the FDA. The FDA is a federal administration that regulates food and drugs. With this said, the FDA uses policies to maintain its control over certain things such as companies that do not follow the rules set forth by the government. The FDA has a process in which they go about getting certain things off of the market to keep people safe; they first send out a warning to said companies and if the companies do not take into account …show more content…

Another instance of the FDA regulating drug administration would be the COVID-19 vaccination. In December 2020 when the COVID vaccination had just recently come out, the FDA gave the authorization for use because of the state of the country at that time. However, they had not approved the vaccine until August 2021. This example could also be used as one of the potential challenges that they may face. I say this because they did not actually approve of the vaccination until it was already distributed to a good part of the country. The challenge of this is that while the vaccination did work it could have gone the other way and the FDA would have been faulted for this because they gave the emergency use authorization. So, therefore, one of the potential challenges the FDA may face is having to make decisions based on emergencies that they cannot control. The FDA also runs the food administration. For example, when you see recalls in stores for certain products it is because the FDA declares them unsafe to the public. Lastly, the FDA controls a large part of the cosmetic industry because they require cosmetics to be accurately labeled and have safe

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271 Words | 2 Pages

Consumers barley read whats in the stuff they are taking in. Not to add, they can not know what they're taking in if it is never writing on the bottle. It is unethical to target these consumers. It could hurt the consumer causing a lawsuit or furthermore shutting down the company. FDA should regulate this kind of stuff so it never happens.

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The FDA is a government agency that had the responsibility to protect the health of the nation from impure and unsafe drugs, food, cosmetics, and other products. The FDA did this by administering the regulation of biological products shipped within the United states and with foreign countries. The FDA must approve all drugs before they can be sold in the United States. It also inspects manufacturing facilities and it tests the products to be sold to make sure they meet the current standards and it

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755 Words | 4 Pages

The FDA was very impactful for quite a few reasons; first, it was a federal agency which could monitor existing and new products much more effectively, and second, it could help further an educational aspect of public health, instructing the general public on how to safely consume food. Again, this institution is still around today, but it was not until the 1970s that real justice and regulations were provided for manual labourers working in factories. In 1970, the Occupational Safety and Health Act was enacted. It ensures employers had to provide secure work environments free from health hazards were provided to all employees. For some activists who had worked for decades on this issue, this legislation and support was a satisfying conclusion.

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This has been reflected in the new Public Health Act in BC, which allows authorities the power to establish directives and regulations for individuals when delivering a public health function (under Section 63). The act attempts to balance the autonomy of individuals and the right action for the public good. [14] In this case, the fine line between the workers’ individual right and freedom and protection of public health has yet to be explored and defined. It appears that the policy was on the reasonable ground that flu shot mandatory protect HCW and patients’ safety from getting flu. I believe that the key issue is to attain evidence-based study to ensure the vaccine safety and effectiveness for both HCW and patients.

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West Encyclopedia (2005) studies show that “The FDA annually regulates over $1 trillion worth of products, which accounts for one-fourth of all consumer spending in the United States.” The FDA protect patients’ rights and safety in clinical trials of new medical products, monitor promotional activities and regulate labeling of packaged foods. The FDA is responsible for monitoring the safety of the nation’s blood supply.

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The Pure Food and Drug Act of 1906, which we have already discussed, was the primary reason the Food and Drug Administration (FDA) was established. This law was created because many people relocated to cities to work in factories and other urban jobs, and because there was little to no workplace or product safety, pre-made goods were required because city dwellers could not produce them themselves. The Food and Drug Administration is responsible for a wide range of duties, including dietary supplements, bottled water, food additives, infant formulas, prescription drugs, non prescription drugs, vaccines for humans, blood and blood products, cellular and gene therapy products, tissue and tissue products, allergenics, heart pacemakers, dental devices, surgical implants and prosthetics, x-ray equipment, ultrasonic therapy equipment, color additives found in makeup and other personal care products, skin moisturizers and cleansers, nail polish and perfume, livestock feeds, pet foods, veterinary drugs and devices, cigarettes, e-cigarettes, and

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An example of this is the Daraprim Scandal. Andrew Pollack, a journalist who has covered the Daraprim Scandal, talks about how the Turing Pharmaceuticals has changed the price of Daraprim from $13.50 to $750 (Pollack para 2). This price change shows how the government has no control over the pharmaceutical industry. Moreover, Martin Shkreli, the chief executive,

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706 Words | 3 Pages

Our FDA has been holding back the cure to a disease that has affected 29.1 million people! You may be thinking there is no way anyone could do this. If you think that you must be forgetting something called money. The FDA not giving up that they have the cure for diabetes and it is getting them and saving them a LOT of money and it would take a lot of time that people might not feel is worth putting in. But you would think that someone would find out and tell everyone, right?

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The FDA stands for Food and Drug Administration. The FDA is controlled by the federal executive department. It was founded in 1906 by President Roosevelt. The purpose of the FDA is to protect and promote good public health nationwide. Originally it started as just a food administration, needed to enforce proper food labeling, then later became a drug administration as well.

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Throughout the 19th century, much of the legislation and oversight of vaccinations fell to the states and local jurisdictions. This included production and distribution of vaccines, enforcement (including penal outcomes) of regulation, and final adjudication of any disputes (Gostin, 2008). In 1902, however the U.S. Congress passed the “Biologics Control Act” (BCA) which set the standards for the first legislation of drugs. This meant that guidance on the production, distribution, and research on vaccines came from the federal level.

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721 Words | 3 Pages

The debate as to the safety of vaccinations is as old as vaccinations. The vaccinations were created to in hopes of protection against dangerous communicable diseases. Time, statistics and evidence has been proved that vaccinations do work. Vaccinations serve one purpose, to save people by reducing the risk of infections and contracting diseases. If people do not get vaccinated, protection is not guaranteed and the risk of irreversible health problems or death is inevitable.

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147 Words | 1 Pages

Vaccinations have come to believe as the most effective, life-saving medical innovation of all time. They have cleared the way of numerous diseases, and they are saving the lives of children and adults every day from infectious diseases. With every lifesaving innovation, critics seem to be required to put doubt in people's mind. A new debate has risen from the minds of the skeptics, and the debate is costing people their lives. The book Vaccine, written by Mark Largent about the recent controversy, states that “about 40% of American parents today have chosen to delay certain vaccines or outright refuse to allow their children’s physicians to vaccinate their children” (Largent 1).

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Vaccination rules need to be changed to prevent a major outbreak of several or one diseases. The CDC can reduce the number of unvaccinated children by creating strict rules that parents must follow. Therefore; the vaccines will be technically forced upon the child if needed and given proper

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Required Immunity Mandatory vaccinations for children in public schools have been the center of much debate since laws were first developed to regulate immunization. Fears from parents about side effects and adverse reactions have steered many away from wanting to vaccinate their children despite the numerous infectious diseases they prevent. These debates have gotten in the way of progression in schools for preventing the spread of disease. To me, the risks of not vaccinating children are far greater than the risks of adverse reactions.

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720 Words | 3 Pages

Many new companies to enter the market without burden of costly tasks such as research and development, clinical trials and manufacturing of drugs. Moreover, patent expiry is one of the reasons which is offering opportunities for lower cost generic manufacturer in terms of greater market access. Additionally, the government has increased their focus on healthcare cost cutting. It is creating pressure on the authority to allow early introduction of low-cost drugs in the

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