Prescription Drugs: Describe and discuss the FDA’s guidelines for safety and efficacy.
US FDA the Food and Drug Administration is a well known federal agency of US basically the Department of Health & Human Services established for the purpose of protecting overall public health considering the safety and efficacy standards of various drugs, food products cosmetics as well as biological products for human as well as veterinary use.
It also regulates the manufacturing, distribution and marketing of these products, controls the misbranded and spurious produces.
It approves the new drug substances under NDA and also bans some products on the basis of set standard violation regarding quality and safety.
Prescription Drugs: Describe and discuss the FDA’s guidelines for safety and efficacy.
Prescription Drugs: Describe and discuss the consequences of price controls on prescription drugs.
Prescription Drugs: Describe and discuss the political attractiveness of price controls on prescription drugs.
Prescription Drugs: Describe and discuss the history of prescription drug regulation.
Prescription Drugs: Describe and discuss why prescription drugs are expected to be priced lower overseas than US.
Prescription Drugs: Describe and discuss the rationale for FDA regulation of drugs.
Prescription Drugs: . Describe and discuss the development of new drugs by the U.S. pharmaceutical industry.
Prescription Drugs: Describe and discuss the structure of the pharmaceutical industry.
Prescription Drugs: Describe and discuss the accuracy of studies on international variations in drug prices.
Prescription Drugs: Describe and discuss the main reasons for the ongoing increases in pharmaceutical expenditures in the United States.
Prescription Drugs: Describe and discuss the rationale for considering the pharmaceutical industry a public policy dilemma.