to formulate Good Laboratory Practice (GLP), Good Clinical Practice (GCP) in consultation with relevant authorities and supervise their implementation;

 
  • 商有關(guān)部門(mén)制定藥物非臨床研究、藥物臨床試驗的質(zhì)量管理規范并監督實(shí)施;
今日熱詞
目錄 附錄 查詞歷史
国内精品美女A∨在线播放xuan