the u. s. food and drug administration is an example of whose interest in health care? course hero

What is the food and Drug Administration responsible for?

The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply

What is the role of the FDA in public health?

The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.

Who is responsible for the safety of Public Health?

State, Local, and Tribal Governments Food and Drug Administration The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.

See more

What is the role of the Food and Drug Administration?

The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation's food supply, cosmetics, and products that emit radiation.

How does the FDA fulfill its responsibility?

FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health threats.

What is a human subject?

According to the federal regulations, human subjects are living individuals about whom an investigator conducting research obtains information through interaction or intervention with the individual, and uses, studies, or analyzes the information; or: Obtains, uses, studies, analyzes, or generates identifiable private information.

What is the only record linking the subject and the research?

The only record linking the subject and the research is the consent document and the principal risk is a breach of confidentiality. As part of the consent process, the federal regulations require researchers to: Provide potential subjects with information at the appropriate reading comprehension level.

What does the IRB have to ensure?

The IRB must ensure that: Confidentiality of the prisoners' health status is maintained. You learn that one of the subjects from your study will be admitted to prison next week. You assert that it is in the best interest of the subject to remain in the study while incarcerated.

What is public health?

The public health concept undergoes numerous discussions and considerable changes around the whole globe. Many public organizations make attempts to improve the health conditions of the population and promote the well-being of people through preventing diseases and prolonging lives (Andrade et al., 2017). Many federal public health agencies work in the chosen field. In this paper, special attention will be paid to the Food and Drug Administration (FDA) and one of its services, tobacco products regulation.

What is the FDA responsible for?

The FDA takes responsibility for the development of safe and effective standards with the help of which it is possible to evaluate tobacco products, their risks, benefits, and possible distribution among the population, both users and non-users. According to the Tobacco Control Act, the US population should be careful with tobacco products in terms of their sales to minors, the support of vending machines, the sale of packages with fewer than 20 cigarettes, tobacco-based sponsorship, social and cultural events, and free giveaways (Food and Drug Administration, 2016). These activities are banned in the United States. The FDA also underlines the necessity to use special warning labels where it is stated that smoking is harmful to human health, starting from tooth loss or addiction and ending with death because of lung cancer.

What is the role of the FDA in tobacco regulation?

Tobacco product regulation is a serious step taken by the FDA to protect people’s health and describe the conditions under which people can understand what they do right and wrong. Tobacco products, as well as the ways of their usage, vary. The task of the FDA is to make sure people follow special standards and respect their health needs. Public health is a broad topic, and the steps show how it can be solved today.

What are the goals of the FDA?

The goals of the FDA concerning tobacco control are also supported by such organizations as the Centers for Disease Control and Prevention, the Institute of Medicine, and even the US Department of Defense. This collaboration is a chance to change human lives at different levels. People should know what is dangerous to them, and the exchange of information at the national level is a good step forward.

What is the purpose of the FDA?

The FDA was organized more than a century ago with the goal to protect and promote public health through food safety control. With time, its goals were changed; still, its mission remains the same –public health support. Regarding this broad mission, the FDA finds it reasonable to create several goals to explain its steps in different fields. The protection of public health is possible by ensuring the safety of human and veterinary drugs, biological products, and radiation-free cosmetics (U.S. Food & Drug Administration, 2018). The FDA is responsible for the regulation of tobacco products and their reduction.

How does the FDA impact human health?

The FDA is a well-known American organization that has an impact on the quality of human life through the promotion of information and clear standards on how to define the safety of food, drugs, tobacco products, and other important health issues. The FDA shows that well-being is not only the control of food, drugs, and medical devices. To be healthy, people have to understand the importance of the use of radiation-emitting products, the participation in vaccination and blood control, the discussion of veterinary affairs, and the evaluation of cosmetics and tobacco products (U.S. Food & Drug Administration, 2018).

Is tobacco a preventable disease?

The representatives of the FDA define tobacco products as one of the largest still preventable causes of death and diseases in the United States of America. Therefore, they find it necessary to fight against this problem using any available methods and means. In 2009, the Family Smoking Prevention and Tobacco Control Act was signed by President Obama to define the responsibilities of the FDA in its intentions to control the progress of the tobacco industry.