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本帖最后由 kslam 于 2017-5-23 23:30 编辑
常州市前药制药原料厂 (江苏省常州市金坛区白塔庄城678号)
FDA进口禁令 "66-40 " 2017年5月4日
违规项目:
1. Failure to implement a system for managing quality encompassing the organizational structure, procedures, processes and resources, as well as activities to ensure confidence that the API will meet its intended specifications for quality and purity. Failure to define and document all quality-related activities.
未能实施质量管理的体系,包括组织结构,程序,流程和资源,以确保API能达到其质量和纯度的预期标准的活动。 未确定和记录所有质量相关的活动。
2. Failure to have adequate written procedures for the receipt, identification, quarantine, storage, sampling, testing, handling, and approval or rejection of raw materials.
未对接收,鉴定,待验,储存,取样,测试,操作和批准或拒绝原辅料的书面程序。
3. Failure to have laboratory control records that include complete data derived from all laboratory tests conducted to ensure compliance with established specifications and standards.
没有实验室控制记录,包括从所有为保证符合既定质量标准检测中产生的完整数据。
4. Failure to prepare adequate batch production records and record the activities at the time they are performed.
未能准备适当批生产记录和未在活动实施的同时进行记录。
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