潔凈廠房外部壞境要驗證嗎?
來源:hardcandy99.cn 發布時間:2022/4/29 16:24:44
潔凈廠房建成之后肯定(ding)需(xu)要進行驗證(zheng),通過之后才可正式(shi)投入(ru)生產(chan),但(dan)就(jiu)是這(zhe)個(ge)驗證(zheng)問題讓很多(duo)人難(nan)辦,不(bu)清楚怎么(me)辦操作,其中(zhong)外部環境(jing)是否(fou)需(xu)要驗證(zheng)?
潔(jie)凈(jing)(jing)(jing)廠(chang)房驗證理應依(yi)據藥物種(zhong)類(lei)、生(sheng)產制造實際(ji)操作規定及外部自(zi)然(ran)環(huan)境(jing)情況(kuang)等配備空氣(qi)凈(jing)(jing)(jing)化系統系統軟件,使(shi)廠(chang)區(qu)(qu)合理自(zi)然(ran)通風,并有溫度(du)(du)、環(huan)境(jing)濕度(du)(du)操縱和(he)空氣(qi)過(guo)濾過(guo)慮,確保藥物的(de)工作環(huan)境(jing)符合規定。潔(jie)凈(jing)(jing)(jing)區(qu)(qu)和(he)非潔(jie)凈(jing)(jing)(jing)區(qu)(qu)中間(jian)、不(bu)一樣等級潔(jie)凈(jing)(jing)(jing)區(qu)(qu)中間(jian)的(de)壓力差(cha)理應不(bu)少于10帕斯卡。必(bi)需(xu)時,同樣潔(jie)凈(jing)(jing)(jing)度(du)(du)等級等級的(de)不(bu)一樣作用地(di)區(qu)(qu)(操作室)中間(jian)也理應維(wei)持適度(du)(du)的(de)壓力差(cha)梯度(du)(du)方向。
一(yi)般來(lai)說,有清潔規(gui)(gui)定(ding)的(de)潔凈(jing)廠房及有關(guan)的(de)空氣(qi)凈(jing)化系(xi)統(tong)(tong)(tong)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)都將被判斷為立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian);一(yi)部分(fen)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)盡管無清潔規(gui)(gui)定(ding),但(dan)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)中的(de)一(yi)部分(fen)主要參數將做為生產工藝(yi)流程的(de)關(guan)鍵性要素,如溫度智能管理(li)系(xi)統(tong)(tong)(tong),包含凍庫、溫室(shi)大(da)棚等,該類系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)也在立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)之列(lie)。除立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)以外(wai)的(de)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian),可(ke)依照(zhao)其實際作用界定(ding)為間(jian)(jian)接性危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)或無危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)。立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)遵照(zhao)GEP規(gui)(gui)定(ding)設(she)計(ji)方(fang)案和(he)調(diao)(diao)節,并依據(ju)GMP規(gui)(gui)定(ding)驗證,間(jian)(jian)接性危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)和(he)無危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)僅遵照(zhao)GEP規(gui)(gui)定(ding)開展設(she)計(ji)方(fang)案和(he)調(diao)(diao)節。
潔(jie)凈(jing)(jing)(jing)廠(chang)房驗證理應依(yi)據藥物種(zhong)類(lei)、生(sheng)產制造實際(ji)操作規定及外部自(zi)然(ran)環(huan)境(jing)情況(kuang)等配備空氣(qi)凈(jing)(jing)(jing)化系統系統軟件,使(shi)廠(chang)區(qu)(qu)合理自(zi)然(ran)通風,并有溫度(du)(du)、環(huan)境(jing)濕度(du)(du)操縱和(he)空氣(qi)過(guo)濾過(guo)慮,確保藥物的(de)工作環(huan)境(jing)符合規定。潔(jie)凈(jing)(jing)(jing)區(qu)(qu)和(he)非潔(jie)凈(jing)(jing)(jing)區(qu)(qu)中間(jian)、不(bu)一樣等級潔(jie)凈(jing)(jing)(jing)區(qu)(qu)中間(jian)的(de)壓力差(cha)理應不(bu)少于10帕斯卡。必(bi)需(xu)時,同樣潔(jie)凈(jing)(jing)(jing)度(du)(du)等級等級的(de)不(bu)一樣作用地(di)區(qu)(qu)(操作室)中間(jian)也理應維(wei)持適度(du)(du)的(de)壓力差(cha)梯度(du)(du)方向。
潔凈廠房(fang)制(zhi)冷機(ji)(ji)組(zu)的(de)調節工程驗(yan)收(參考GB/T14294-2008整體式制(zhi)冷機(ji)(ji)組(zu)),1、文檔查驗(yan)(現行標準(zhun)、合理、齊備),2、安(an)裝記錄查驗(yan)(工程監理紀錄),3、關鍵零部(bu)件查驗(yan)(規格(ge)型號恰(qia)當(dang)(dang),構件齊備),4、構造和(he)外(wai)型查驗(yan)(符(fu)合規定),5、公共(gong)工程項目查驗(yan)(當(dang)(dang)場(chang)安(an)裝與設計方案保持一(yi)致(zhi)),6、制(zhi)冷機(ji)(ji)組(zu)透(tou)風(feng)量檢(jian)測(ce)。取一(yi)外(wai)部(bu)離(li)心(xin)風(feng)機(ji)(ji),與制(zhi)冷機(ji)(ji)組(zu)連接,將制(zhi)冷機(ji)(ji)組(zu)其(qi)他張口一(yi)部(bu)分堵漏嚴實(shi),應(ying)用外(wai)補離(li)心(xin)風(feng)機(ji)(ji)對制(zhi)冷機(ji)(ji)組(zu)開展(zhan)打擊(ji),在保壓1000Pa的(de)標準(zhun)下,測(ce)量外(wai)部(bu)離(li)心(xin)風(feng)機(ji)(ji)送(song)排風(feng)量。
一(yi)般來(lai)說,有清潔規(gui)(gui)定(ding)的(de)潔凈(jing)廠房及有關(guan)的(de)空氣(qi)凈(jing)化系(xi)統(tong)(tong)(tong)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)都將被判斷為立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian);一(yi)部分(fen)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)盡管無清潔規(gui)(gui)定(ding),但(dan)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)中的(de)一(yi)部分(fen)主要參數將做為生產工藝(yi)流程的(de)關(guan)鍵性要素,如溫度智能管理(li)系(xi)統(tong)(tong)(tong),包含凍庫、溫室(shi)大(da)棚等,該類系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)也在立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)之列(lie)。除立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)以外(wai)的(de)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian),可(ke)依照(zhao)其實際作用界定(ding)為間(jian)(jian)接性危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)或無危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)。立即(ji)(ji)危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)遵照(zhao)GEP規(gui)(gui)定(ding)設(she)計(ji)方(fang)案和(he)調(diao)(diao)節,并依據(ju)GMP規(gui)(gui)定(ding)驗證,間(jian)(jian)接性危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)和(he)無危(wei)害(hai)系(xi)統(tong)(tong)(tong)軟(ruan)(ruan)件(jian)(jian)(jian)僅遵照(zhao)GEP規(gui)(gui)定(ding)開展設(she)計(ji)方(fang)案和(he)調(diao)(diao)節。
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