IRB/FDA
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IRB/FDA
Medical science occupies a dark area of human history, with doctors akin to the likes of the fictional Dr. Frankenstien. The problem was the need to experiment on humans. Medicine deals with the prevention of death. To do so, it must investigate and understand the mechanisms of death. However, there also needs to be strict scientific standards to protect patients from bad science and medical mistakes. This is the function of an IRB (Institutional Review Board). The largest of which is the FDA (The Food & Drug Administration). The FDA regulates all drugs and medical proceedure in the United States, and since most of the world's medicine is developed in the United States - the FDA also acts as the world's IRB. However, the drug failures of Vioxx and other such drugs, in November of 2004, highlighted a need to expand the IRB/FDA standard to the global level. This is the function of this IRB, to develop and provide a global standard to ensure patient safety.
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