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目录1
概述··········································································································································32
再验证目的··························································································································33
引用标准·······························································································································34
验证组织职责·····················································································································45
进度计划·······························································································································56
验证实施的步骤和要求···············································································
