Under present federal regulation, a pharmaceutical company that is attempting to gain Food and Drug Administration (FDA) approval for marketing a new drug is responsible for conducting the necessary drug experimentation. It has been forcefully argued that because the company has a financial interest in successful test results, the present drug testing system contains an inherent bias that adversely affects the accuracy and acceptability of drug research. Concern about these effects has led to proposals that pharmaceutical research be conducted by independent parties with no financial interest in the outcome of the research. To evaluate whether such regulatory changes are necessary, this Article will examine the relationship between the pr...
The government, particularly the Food and Drug Administration ( FDA ), heavily regulates the life sc...
The FDA employs an average-patient standard when reviewing drugs: it approves a drug only if is safe...
Congress is considering legislation that would create an abbreviated FDA approval process for follow...
Under present federal regulation, a pharmaceutical company that is attempting to gain Food and Drug ...
R&D of new drugs is driven by pharmaceutical companies that invest considerable amounts of money for...
This Article explores a proposal that would preclude biased drug testing by removing all drug sponso...
Pharmaceutical companies often replace prescription drugs that are already on the market with modifi...
Innovation does not stop when new medicines are launched. Companies with approved drugs and biologic...
Although radical changes in drug regulation are rare (e.g., the Federal Food, Drug and Cosmetic Act ...
The Food and Drug Administration’s (FDA) drug approval process carries great significance for both p...
The aim of this research is to know what FDA was done to get pure food and drug. Was it to put all t...
Concerns about potentially misleading reporting of pharmaceutical industry research have surfaced ma...
Sometimes drug innovation seems to happen in reverse. Patients enjoy a treatment for years even thou...
The U.S. Congress passed the Kefauver-Harris Amendments to the Food, Drug, and Cosmetic Act in 1962....
Uncovering the secrets of nature and mak-ing a profit are distinct motivations for conducting and re...
The government, particularly the Food and Drug Administration ( FDA ), heavily regulates the life sc...
The FDA employs an average-patient standard when reviewing drugs: it approves a drug only if is safe...
Congress is considering legislation that would create an abbreviated FDA approval process for follow...
Under present federal regulation, a pharmaceutical company that is attempting to gain Food and Drug ...
R&D of new drugs is driven by pharmaceutical companies that invest considerable amounts of money for...
This Article explores a proposal that would preclude biased drug testing by removing all drug sponso...
Pharmaceutical companies often replace prescription drugs that are already on the market with modifi...
Innovation does not stop when new medicines are launched. Companies with approved drugs and biologic...
Although radical changes in drug regulation are rare (e.g., the Federal Food, Drug and Cosmetic Act ...
The Food and Drug Administration’s (FDA) drug approval process carries great significance for both p...
The aim of this research is to know what FDA was done to get pure food and drug. Was it to put all t...
Concerns about potentially misleading reporting of pharmaceutical industry research have surfaced ma...
Sometimes drug innovation seems to happen in reverse. Patients enjoy a treatment for years even thou...
The U.S. Congress passed the Kefauver-Harris Amendments to the Food, Drug, and Cosmetic Act in 1962....
Uncovering the secrets of nature and mak-ing a profit are distinct motivations for conducting and re...
The government, particularly the Food and Drug Administration ( FDA ), heavily regulates the life sc...
The FDA employs an average-patient standard when reviewing drugs: it approves a drug only if is safe...
Congress is considering legislation that would create an abbreviated FDA approval process for follow...