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Food quality importance to the food industry
Importance of food quality evaluation
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The Food and Drug Administration, also known as the FDA or USFDA, is responsible for protecting and advocating public health. The mission of the Food & Drug Administration is to enforce laws enacted by the U.S. Congress and regulations established by the Agency to protect the consumer's health, safety, and overall well-being. The FDA has worked for years to establish safety standards for companies to adhere to, in hopes of improving public health. Existing for more than a hundred years, the FDA impacts the health industry through their laws and practices, all of which manage the safety of this country. The FDA is an agency within the Department of Health and Human Services. The FDA is organized through the Office of the Commissioner as well
The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products.
1. Federal Aviation Administration (FAA) - Has the authority to regulate and oversee all aspects of American civil aviation: (Wikipedia contributors, 2014).
According to the 2002 Harris poll, seven out of ten adults in the United States take vitamins, minerals, herbs, or other supplements (Schardt 2). Due to media advertising, dietary supplements are becoming more popular. Companies compete to have the best supplements. It is said that forty percent of American adults take vitamin supplements and over the counter products, which total in several billion dollars (Farley 2). Although many of the supplements claim to be healthy and help lose weight, the dangers are endless. Dietary supplements can be illegally spiked and are not safe. Therefore, putting regulations on dietary supplements and their safety hazards is necessary.
Why do consumers purchase specific drugs for various ailments, sicknesses or diseases they might have? Why do physicians prescribe certain drugs over competitive drugs that may be available to the public? Why is it that most of us can easily name specific drugs that fit the many ailments of today’s society? On the surface the answer might be as simple as good TV advertising or radio commercials or even internet adds. The truth of matter is the major pharmaceutical manufacturers own the patents on these drugs and this gives them all of the marketing budget and muscle they need to promote the drug and control the pricing. The incentives for larger pharmaceutical companies are very enticing and as a result, they don’t mind spending the time in clinical trials and patent courts to get their drugs approved. Some will even get patents on the process by which the drug is manufactured, ensuring that no competitor can steal the drug or the process. This protects their large financial investment and nearly guarantees a large return for their investors. Many consumer rights groups claim this is nothing more than legalizing monopolies for the biggest manufacturers.
The FDA says that they test there medicines on healthy patients but hundreds of people die from simple mistakes like not watching each person side effect and report the correct information in clinical reports. NO criminal charges were faced to Johnson and Johnson and I think some criminal charges or a settlement for patients who experienced the side effects that the drug Risperdal caused. Each year the FDA take 100,000 people lives from taking medicines that are being approved by the FDA. Who is the FDA truly protecting and what responsibilities does the FDA accept due to the fact that more deaths are led by drugs that are approved by the FDA. The FDA say there for the people but are they really thinking about the lives there taking or the money that their gaining from the drugs they approve each year. The FDA is responsible for protecting the public health by ensuring that human and veterinary drug, and vaccines and other biological products and medical devices intended for human use are safe and effective. The FDA should no longer approve medicines that may cause severe side effects or in some cases death; drugs who manufacture these medications should face criminal
The FDA stands for The Food and Drug Administration. The FDA is an agency of the
Every year approximately 200,000 souls die from prescription drug reactions, with another 80,000 dying from medical malpractice (The International). Where is the FDA based? Why do they continue to allow doctors to prescribe these drugs? How could they get to this point? What once was believed to be a panacia for depression has turned into Pandora's box (Tracy).
Healthcare services should be provided to all people without discriminations of any nature. Professionals in the healthcare sector should ensure that while attending to patients, they act in accordance to the medical laws. Agencies regulating the healthcare industry ensure that all the health professionals act in accordance to the medical laws and people have access to high quality medical attention.
...ous tests (Law, 2004). They also must now have the FDA’s approval in order for a certain food or drug to be sold directly to consumers. Also the marketplace has changed, due to new ways to process the product in a more safe and effective manner. There were also changes due to political, economical, social, and cultural changes since 1906. In conclusion, the Food and Drug Act paved the way for the Progressive movement and food safety in America.
Dr. Mercola, an osteopathic physician exclaims that the only reason the government wants regulations on supplements is to have power over consumers (par. 3). Mercola explains that if dietary supplements are bad for public health then why the government is not taking action for other substances that are considered dangerous, “You don't see Durbin beating down the door of Starbucks or Dunkin Donuts, even though coffee is the primary source where most people get their caffeine fix” (Mercola, par. 5). Furthermore the Dietary Supplement Health and Education Act (DSHEA) is doing enough to regulate the dietary supplements. As stated on the DSHEA mission, “DSHEA grants the FDA the authority to regulate dietary supplements in to important respects” (“Dietary Supplements…par. 3). DSHEA does give the FDA the right to regulate many different types of dietary supplements, so there are some regulations to keep Americans healthy and happy without taking away the freedom to purchase these products at a
The agency’s primary responsibility is to be the chief health policy and planning entity for the state. The department is responsible for health facility licensure, inspection, and regulatory enforcement; investigation of consumer complaints related to health care facilities and managed care plans; the implementation of the certificate of need program; the operation of the Florida Center for Health Information a...
There are many federal agencies in the United State of America. Majority of agencies are executive branch agencies such as United States Department of Veterans Affairs. The Department of Veterans Affairs is one of the most important agencies in our nation. Moreover, they have history, mission, structure, and powers since they help and take care our veterans.
FDAs public health protection duties. By ensuring that products and producers meet certain standards, FDA protects consumers and enables them to know what they are
Health care laws and regulations influence the delivery of health care services in the United States. Health regulation and regulations agencies develop and enforce laws to protect and improve the access to affordable health care for all Americans. Regulatory agencies affect health care organizations, health care providers, drug and pharmaceutical companies, and health care research.
...ly look at the false claims made by food industries expand on their already set regulations, making it harder for companies to get around them. However, if the FDA believes that their regulations are as specific as they can get, then there should be at least somebody to educate consumers about food labels and add more detail to nutritional value charts. Because without changing the way how information is provided and educating people, they will not be able to change their diets to improve nations overall health.