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These techniques are needed for any drug trials on humans, but research involving Agenda I prescription drugs have supplemental requirements in the Drug Enforcement Administration.
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This protocol is judged by an institutional evaluate board, an unbiased group that critiques any clinical trials involving people. If a research entails a Agenda I drug, as soon as the board approves the protocol as moral, the scientists should make an application for an investigational new drug (IND) number from your FDA.