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“It will take various months in some cases to get it carried out, but I don’t think scientists will shy clear of performing Timetable I study due to the necessities if it fascinates them,” Halpern explained to me.
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This protocol is judged by an institutional overview board, an impartial team that assessments any scientific trials involving individuals. If a review entails a Timetable I drug, after the board approves the protocol as ethical, the scientists should submit an application for an investigational new drug (IND) number from the FDA.