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FDA对中国药科大学仪器分析中心发出警告信:合规性挑战与行业启示
实验记录仅包含两行数字,缺乏样品制备方法、测试步骤、系统适用性等关键信息(违反21 CFR 211.194(a))。 2023年11月之前的数据存储在外部硬盘中,难以调取(违反21 CFR 211.180(c))。 计算机系统缺乏权限控制,多名用户共享一个具有完全管理权限的登录ID(违反 ...
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