文章來源：中(zhong)(zhong)國中(zhong)(zhong)化(hua)集團公(gong)司 發布時間：2008-12-07
近日(ri)，在(zai)全(quan)(quan)國農(nong)藥登記(ji)毒理學試驗管(guan)理工作會議(yi)上，中(zhong)國中(zhong)化集團(tuan)公(gong)司（簡稱(cheng)“中(zhong)化集團(tuan)”）下屬企業(ye)(ye)沈陽化工研究院（簡稱(cheng)“沈陽院”）的安全(quan)(quan)評價中(zhong)心獲得A級(ji)資質(zhi)。此次會議(yi)由沈陽院安全(quan)(quan)評價中(zhong)心與農(nong)業(ye)(ye)部農(nong)藥檢定(ding)所共同舉辦，全(quan)(quan)國35家毒理學試驗單位獲得了資質(zhi)證書。
沈(shen)(shen)陽(yang)院安(an)(an)全(quan)(quan)評(ping)價(jia)中(zhong)(zhong)心主(zhu)要從事(shi)農(nong)(nong)(nong)藥(yao)(yao)(yao)、醫藥(yao)(yao)(yao)及其它精細(xi)化(hua)(hua)學品的(de)安(an)(an)全(quan)(quan)性研究(jiu)(jiu)工作，擁有每(mei)年實(shi)施1200多個實(shi)驗(yan)項目的(de)能(neng)力(li)，是目前國(guo)(guo)(guo)(guo)內(nei)唯一能(neng)夠同(tong)時(shi)從事(shi)農(nong)(nong)(nong)藥(yao)(yao)(yao)、醫藥(yao)(yao)(yao)以(yi)及化(hua)(hua)學品的(de)安(an)(an)全(quan)(quan)評(ping)價(jia)試驗(yan)機(ji)構。近年來，沈(shen)(shen)陽(yang)院安(an)(an)全(quan)(quan)評(ping)價(jia)中(zhong)(zhong)心積極探索與(yu)國(guo)(guo)(guo)(guo)際接軌(gui)，推進GLP（Good Laboratory Practice）實(shi)驗(yan)室(shi)建(jian)(jian)設，建(jian)(jian)成了接近國(guo)(guo)(guo)(guo)際水(shui)準的(de)安(an)(an)全(quan)(quan)評(ping)價(jia)機(ji)構，先后被國(guo)(guo)(guo)(guo)家(jia)(jia)認證(zheng)為“化(hua)(hua)學工業農(nong)(nong)(nong)藥(yao)(yao)(yao)安(an)(an)全(quan)(quan)評(ping)價(jia)質量監督檢驗(yan)中(zhong)(zhong)心”和(he)“國(guo)(guo)(guo)(guo)家(jia)(jia)沈(shen)(shen)陽(yang)新藥(yao)(yao)(yao)安(an)(an)全(quan)(quan)評(ping)價(jia)研究(jiu)(jiu)中(zhong)(zhong)心”，在(zai)2006年又通(tong)過了國(guo)(guo)(guo)(guo)家(jia)(jia)實(shi)驗(yan)室(shi)認可委(wei)員(yuan)會(hui)的(de)國(guo)(guo)(guo)(guo)家(jia)(jia)實(shi)驗(yan)室(shi)認證(zheng)檢查(cha)及美國(guo)(guo)(guo)(guo)AAALAC（國(guo)(guo)(guo)(guo)際實(shi)驗(yan)動物(wu)委(wei)托和(he)評(ping)估委(wei)員(yuan)會(hui)）的(de)正式認證(zheng)檢查(cha)。此次與(yu)農(nong)(nong)(nong)業部農(nong)(nong)(nong)藥(yao)(yao)(yao)檢定所共同(tong)舉辦(ban)全(quan)(quan)國(guo)(guo)(guo)(guo)農(nong)(nong)(nong)藥(yao)(yao)(yao)登記毒(du)理學試驗(yan)管理工作會(hui)議及有關(guan)培訓活(huo)動，進一步鞏固和(he)提升(sheng)了沈(shen)(shen)陽(yang)院安(an)(an)全(quan)(quan)評(ping)價(jia)中(zhong)(zhong)心在(zai)我國(guo)(guo)(guo)(guo)農(nong)(nong)(nong)藥(yao)(yao)(yao)GLP實(shi)驗(yan)室(shi)建(jian)(jian)設以(yi)及毒(du)理學試驗(yan)能(neng)力(li)等方面的(de)領先地位。
GLP是針對試驗研究計劃、試驗操作、監督、記錄和試驗報告等一系列試驗流程的管理而制定的法規性文件，旨在嚴格控制各類化學品安全性評價試驗的各個環節，確保試驗結果的真實性。