纯蒸汽灭菌验证方案

纯蒸汽灭菌验证方案

ID:866803

大小:343.03 KB

页数:18页

时间:2017-09-21

纯蒸汽灭菌验证方案_第1页
纯蒸汽灭菌验证方案_第2页
纯蒸汽灭菌验证方案_第3页
纯蒸汽灭菌验证方案_第4页
纯蒸汽灭菌验证方案_第5页
资源描述:

《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

当前文档最多预览五页,下载文档查看全文

此文档下载收益归作者所有

当前文档最多预览五页,下载文档查看全文
温馨提示:
1. 部分包含数学公式或PPT动画的文件,查看预览时可能会显示错乱或异常,文件下载后无此问题,请放心下载。
2. 本文档由用户上传,版权归属用户,天天文库负责整理代发布。如果您对本文档版权有争议请及时联系客服。
3. 下载前请仔细阅读文档内容,确认文档内容符合您的需求后进行下载,若出现内容与标题不符可向本站投诉处理。
4. 下载文档时可能由于网络波动等原因无法下载或下载错误,付费完成后未能成功下载的用户请联系客服处理。