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・ Regulation of genetically modified organisms in Switzerland
・ Regulation of genetically modified organisms in the European Union
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・ Regulation of Investigatory Powers Act 2000
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・ Regulation of Railways Act 1868
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・ Regulation of therapeutic goods
Regulation of therapeutic goods in the United States
・ Regulation of tobacco by the U.S. Food and Drug Administration
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Regulation of therapeutic goods in the United States : ウィキペディア英語版
Regulation of therapeutic goods in the United States

__NOTOC__
Regulation of therapeutic goods in the United States is carried out by the U.S. Food and Drug Administration (FDA), which makes some drugs available over the counter at retail outlets and others by prescription only.
The possession of some substances is prohibited by scheduling under the Controlled Substances Act, under the joint jurisdiction of the FDA and the Drug Enforcement Administration (DEA)
==Pharmacovigilance==
Three primary branches of pharmacovigilance in the U.S. include the FDA, the pharmaceutical manufacturers, and the academic/non-profit organizations (such as RADAR and Public Citizen).

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