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These techniques are needed for any drug trials on individuals, but research involving Agenda I medicine have supplemental demands in the Drug Enforcement Administration.
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This protocol is judged by an institutional overview board, an impartial group that critiques any clinical trials involving individuals. If a examine requires a Timetable I drug, when the board approves the protocol as moral, the scientists really have to apply for an investigational new drug (IND) range with the FDA.