文章(zhang)來(lai)源：中(zhong)國中(zhong)化集團(tuan)公司(si) 發(fa)布(bu)時間(jian)：2008-12-07
近(jin)日，在全(quan)國(guo)農(nong)藥(yao)登記(ji)毒(du)理學(xue)試(shi)(shi)驗(yan)管(guan)理工作(zuo)會議(yi)上，中國(guo)中化(hua)集(ji)(ji)團公司（簡(jian)稱“中化(hua)集(ji)(ji)團”）下屬(shu)企業沈(shen)陽(yang)(yang)化(hua)工研究院(yuan)（簡(jian)稱“沈(shen)陽(yang)(yang)院(yuan)”）的安全(quan)評(ping)價(jia)中心(xin)獲得A級資質(zhi)。此次(ci)會議(yi)由沈(shen)陽(yang)(yang)院(yuan)安全(quan)評(ping)價(jia)中心(xin)與農(nong)業部農(nong)藥(yao)檢定(ding)所共(gong)同舉辦，全(quan)國(guo)35家毒(du)理學(xue)試(shi)(shi)驗(yan)單位獲得了資質(zhi)證(zheng)書(shu)。
沈(shen)陽(yang)(yang)院(yuan)安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)中(zhong)心(xin)主要從事(shi)農藥(yao)、醫藥(yao)及(ji)(ji)其它精細化學(xue)品(pin)的安(an)(an)(an)全(quan)(quan)性研究工(gong)作，擁有每(mei)年(nian)實(shi)(shi)施1200多個(ge)實(shi)(shi)驗(yan)(yan)項目的能(neng)(neng)力，是(shi)目前國(guo)內唯一(yi)能(neng)(neng)夠同時從事(shi)農藥(yao)、醫藥(yao)以及(ji)(ji)化學(xue)品(pin)的安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)試驗(yan)(yan)機(ji)(ji)構。近(jin)年(nian)來，沈(shen)陽(yang)(yang)院(yuan)安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)中(zhong)心(xin)積極探索與(yu)國(guo)際接軌，推進GLP（Good Laboratory Practice）實(shi)(shi)驗(yan)(yan)室(shi)建(jian)設，建(jian)成了接近(jin)國(guo)際水準的安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)機(ji)(ji)構，先(xian)后被國(guo)家認(ren)證(zheng)為“化學(xue)工(gong)業(ye)農藥(yao)安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)質量(liang)監(jian)督檢(jian)(jian)(jian)驗(yan)(yan)中(zhong)心(xin)”和(he)“國(guo)家沈(shen)陽(yang)(yang)新藥(yao)安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)研究中(zhong)心(xin)”，在2006年(nian)又通(tong)過了國(guo)家實(shi)(shi)驗(yan)(yan)室(shi)認(ren)可(ke)委員會的國(guo)家實(shi)(shi)驗(yan)(yan)室(shi)認(ren)證(zheng)檢(jian)(jian)(jian)查(cha)及(ji)(ji)美國(guo)AAALAC（國(guo)際實(shi)(shi)驗(yan)(yan)動(dong)物委托和(he)評(ping)估委員會）的正(zheng)式認(ren)證(zheng)檢(jian)(jian)(jian)查(cha)。此次(ci)與(yu)農業(ye)部農藥(yao)檢(jian)(jian)(jian)定所共同舉辦全(quan)(quan)國(guo)農藥(yao)登記毒(du)理學(xue)試驗(yan)(yan)管理工(gong)作會議及(ji)(ji)有關培訓活(huo)動(dong)，進一(yi)步(bu)鞏固和(he)提(ti)升了沈(shen)陽(yang)(yang)院(yuan)安(an)(an)(an)全(quan)(quan)評(ping)價(jia)(jia)中(zhong)心(xin)在我(wo)國(guo)農藥(yao)GLP實(shi)(shi)驗(yan)(yan)室(shi)建(jian)設以及(ji)(ji)毒(du)理學(xue)試驗(yan)(yan)能(neng)(neng)力等方面的領先(xian)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。