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These actions are essential for any drug trials on humans, but analysis involving Agenda I prescription drugs have further prerequisites with the Drug Enforcement Administration.
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This protocol is judged by an institutional review board, an unbiased group that assessments any scientific trials involving human beings. If a study consists of a Timetable I drug, once the board approves the protocol as moral, the researchers should make an application for an investigational new drug (IND) amount with the FDA.
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