摘要：为进一步推进GLP的实施，加强实施GLP的监督管理，提高药物安全性评价研究水平，SFDA药品安全监管司将于2006年7～10月对药物非临床安全性评价研究实验室实施GLP的情况进行调研。调研采用问卷调查、现场调研和座谈会相结合的方式进行。
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