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中國(guó)醫(yī)藥企業(yè)制劑國(guó)際化
成為安徽省醫(yī)藥行業(yè)協(xié)會(huì)理事單位
通過(guò)MHRA的首次GMP現(xiàn)場(chǎng)檢查并獲得歐盟GMP證書(shū)
成為中國(guó)第12家通過(guò)歐盟GMP認(rèn)證的固體制劑制藥企業(yè)
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