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时间:2017-09-21
《纯蒸汽灭菌验证方案》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、针剂车间CG-0.6型纯蒸汽灭菌柜再验证方案编定人审核人批准人药业有限公司目录1.概述··········································································································································32.再验证目的·············································································
2、·············································33.引用标准·······························································································································34.验证组织职责··············································································
3、·······································45.进度计划·······························································································································56.验证实施的步骤和要求················································································
4、···············56.1预确认···································································································································56.2运行确认·········································································································
5、·····················56.3性能确认······························································································································57.异常情况处理程序····································································································
6、·····58.拟定验证周期·····················································································································69.结果与评定··························································································································61、概述
7、针剂车间CG-0.6型纯蒸汽灭菌柜是一种全自动的灭菌器。选用先进的微机可编程序控制器进行全程自动控制,密封门的开关锁紧实电动操作。是我公司注射剂车间的器具灭菌专用设备。该灭菌器于2004年安装,2005年通过GMP认证并于2010年通过了GMP再认证,现根据验证要求进行再验证。2、验证目的:2.1确认本设备能够正常运行符合安装要求,各项性能指标符合生产工艺要求。2.2提供必要的文件以证实本设备操作与所预期的完全一致。2.3确认本方案所制定的操作程序及验证方案,能有效地使本设备处于确认状态下,并能稳定地、恒常地达成其所预期的功能
8、。3、引用标准:《药品生产质量管理规范》国家药品监督管理局2010年《药品生产验证指南》国家食品药品监督管理局2003版《验证管理规程》《CG-0.6型纯蒸汽灭菌柜标准操作规程》《CG-0.6型纯蒸汽灭菌柜维护保养标准操作规程》4、验证组织职责4.1.验证领导小组:4.1.1
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