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This protocol is judged by an institutional assessment board, an independent team that testimonials any medical trials involving humans. If a research involves a Routine I drug, once the board approves the protocol as moral, the scientists really have to make an application for an investigational new drug (IND) variety through the FDA.Some research

- 위/변조된 신분증으로 대리시험을 치르거나 치르도록 하는 행위 - 문제를 메모 하고나 녹음하는 행위, 혹은 문제지를 유출하거나 복사하는 행위 - 시험 중 타인의 답안지를 엿보거나 타인에게 보여주는 행위 - 기타 감독관의 규정에 따른 지시에 이유없이 따르지 �