The institutions for non-clinical safety evaluation and study and for clinical study institutions shall respectively follow the Good Laboratory Practice for Non-Clinical Laboratory Studies (GLP) and Good Clinical Practice (GCP).
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- 藥物的非臨床安全性評價(jià)研究機構和臨床試驗機構必須分別執行藥物非臨床研究質(zhì)量管理規范、藥物臨床試驗質(zhì)量管理規范。