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But that compact distinction implies investigate on Plan I medications requires a few added hoops that investigate on other medications don’t. The first step will be to pen a protocol for any study: a system for how the researchers plan to conduct their investigation.

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This protocol is judged by an institutional review board, an independent group that critiques any scientific trials involving individuals. If a analyze will involve a Program I drug, as soon as the board approves the protocol as moral, the researchers must apply for an investigational new drug (IND) quantity from the FDA.