The FDA is the administrative agency that oversees the food and drug industry in America. There...

The FDA is the administrative agency that oversees the food and drug industry in America. There are two types of administrative agencies. Identify the two types of administrative agencies, and identify what makes them different. What types of administrative agency is the FDA and what are the functions of the FDA?

Expert Solution

There are 2 types of administrative agencies.

1.executive agencies

2.independent regulatory agencies .

These two are different.because executive agencies are generally located within the executive branch,under one of the cabinet level departments While independent regulatory agencies exist outside of the federal executive departments.

* the FDA belongs to executive agencies.

* the functions of FDA are

protecting and promoting public health through the control and supervision of food safety,tobacco products ,dietary suppliments,prescription and over-the counter pharmaceutical drugs.
Plays a significant role in the nation's counterterrorism capability.
FDA is responsible for advancing the public health by helping to speed innovations that make medical products more effective ,safer,and more affordable.
Has responsible for regulating the manufacturing ,marketing and distribution of tobacco products to protect the public health.

Nightingale answered 2 years ago

The Food and Drug Administration (FDA) is an agency of the United States Department of Health...

The Food and Drug Administration (FDA) is an 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, prescriptions, and other health-related products. The following are a few examples of the powers the FDA has: • Most federal laws concerning the FDA are part of the Food, Drug, and Cosmetic Act....

3. What government agency oversees the securities industry?

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug should contain less than 25mg of the active ingredient “toxin”, which is assumed to have dangerous side effects. The FDA would like to restrict the error of “approving the drug despite its too high content of toxin” to a maximum risk of 5% (α ≤ 0.05). Let Xi : “ The content of toxin in the i-th pill [in mg].” ∼ N(µ, σ2 )...

A drug company applied for the approval of the Food and Drug Administration (FDA) to market...

A drug company applied for the approval of the Food and Drug Administration (FDA) to market a miracle drug that the company believed could cure some cancers. During the period that the application was under consideration the company's stock rose to $65 per share. The president of the company learned that the FDA application was about to be denied. You are a personal friend of the president, and he told you that he believed that the stock will start trading...

The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations,...

The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations, manufacturers are required to list the amounts of certain nutrients in their foods, such as calories, sugar, fat, and carbohydrates. This nutritional information is displayed on the food’s package. Calories (C) Sugar (S) Fat (F) Carbohydrates (R) 100 12 0.5 25 130 11 1.5 29 100 1 2 20 130 15 2 31 130 13 1.5 29 120 3 0.5 26 100 2 0...

Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is...

Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is too easy and, as a result, too many drugs are approved that are later found to be pushed for a more lenient approval process so that pharmaceutical companies can get new drugs approved more easily and quickly. Consider a null hypothesis that a new, unapproved drug is unsafe and an alternative hypothesis that a new, unapproved drug is safe. Differentiate Type 1 and Type...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to contain specific levels of microbial inhibitors or acidifying agents such as phosphoric or citric acid to prevent production of Clostridium botulinum toxin in the product? (NOTE: An anaerobic environment is present in both bottled and canned products. ) Hint: Look at the lecture slides that discuss how some of these products are made. You can also look up specific information for these items on...

It was recently announced that the Food and Drug Administration (FDA) will extend its regulatory authority...

It was recently announced that the Food and Drug Administration (FDA) will extend its regulatory authority to E-cigarettes, tobacco pipes, and cigars. They have proposed a ban of these products to those under 18 (in person and Internet sales), those purchasing these products must show identification, a ban on use in public places, and products must include warning labels. The producers of cigars and e-cigarettes must register with the FDA, provide a detailed accounting of their product ingredients, disclose their...

The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution,...

The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution, Caridex, which disolves cavities. In a study conducted by dental researchers at Northwestern University, 21 of the 35 patients with cavities preffered treatment with Caridex to drilling (Gainesville Sun, Feb. 11, 1988). Find a 90% confidence interval for the true proportion of dental patients who prefer having cavities dissolved with Caridex rather than drilled. (0.46,0.74) (0.44,0.76) (0.39,0.81)

Question

The FDA is the administrative agency that oversees the food and drug industry in America. There...

Solutions

Expert Solution

Related Solutions

The Food and Drug Administration (FDA) is an agency of the United States Department of Health...

3. What government agency oversees the securities industry?

The Food and Drug Administration (FDA) is asked to approve a new drug. The new drug...

A drug company applied for the approval of the Food and Drug Administration (FDA) to market...

The U.S. Food and Drug Administration (FDA) requires nutrition labeling for most foods. Under FDA regulations,...

Many consumer groups feel that the U.S. Food and Drug Administration (FDA) drug approval process is...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...

1. The The Food and Drug Administration (FDA) requires which ONE of the following products to...

It was recently announced that the Food and Drug Administration (FDA) will extend its regulatory authority...

The U.S. Food and Drug Administration (FDA) recently approved the marketing of a new chemical solution,...