Prescription Drugs: Describe and discuss the rationale for FDA regulation of drugs.
The key rational behind the FDA regulation of the drugs is to ensure the quality of the drug produces as per the regulatory standards for the safety and thus following the regulatory norms of manufacturing, testing, distribution, sales and import and export avoiding the adulteration, misbranding and production of spurious medication.
By imposing the rules and regulation on the drug produces FDA controls the quality of the drugs as these are directly related to the human health and affecting the humanity.
Prescription Drugs: Describe and discuss the rationale for FDA regulation of drugs.
Prescription Drugs: Describe and discuss the history of prescription drug regulation.
Prescription Drugs: Describe and discuss the rationale for considering the pharmaceutical industry a public policy dilemma.
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.
Chapter Three: 6. Discuss federal Food and Drug Administration (FDA) regulation of new drugs.
Prescription Drugs: Describe and discuss why prescription drugs are expected to be priced lower overseas than US.
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 FDA’s guidelines for safety and efficacy.
Prescription Drugs: Describe and discuss the accuracy of studies on international variations in drug prices.