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By Joel Ross | January 11, 2008
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In compliance with government laws and regulations, a medication must undergo a series of research studies to prove that it is safe and effective for a designated medical condition. After all research is completed, a new drug application is submitted to the Food and Drug Administration (FDA) for review. If the FDA determines that the medication or treatment is safe and effective, it grants marketing approval.
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Topics: Clinical Research Study | No Comments »