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These measures are needed for any drug trials on people, but investigation involving Program I medications have further specifications from the Drug Enforcement Administration.
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This protocol is judged by an institutional assessment board, an impartial team that reviews any medical trials involving human beings. If a review consists of a Plan I drug, as soon as the board approves the protocol as ethical, the scientists need to submit an application for an investigational new drug (IND) range from the FDA.