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But that small change means research on Agenda I medicine requires a several added hoops that research on other medicine don’t. The first step will be to pen a protocol for any analyze: a prepare for the way the researchers intend to perform their investigation.
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This protocol is judged by an institutional assessment board, an impartial group that critiques any clinical trials involving humans. If a research requires a Timetable I drug, after the board approves the protocol as ethical, the researchers have to apply for an investigational new drug (IND) number from the FDA.