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“It might take a number of months in some cases to get it completed, but I don’t believe researchers will shy faraway from doing Schedule I study because of the necessities if it fascinates them,” Halpern instructed me.
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This protocol is judged by an institutional assessment board, an independent group that evaluations any scientific trials involving humans. If a review consists of a Timetable I drug, after the board approves the protocol as moral, the scientists have to submit an application for an investigational new drug (IND) number from your FDA.