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发表于 2016-12-7 13:16:54
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中国GMP的要求:
第八十六条 用于药品生产或检验的设备和仪器,应当有使用日志,记录内容包括使用、清洁、维护和维修情况以及日期、时间、所生产及检验的药品名称、规格和批号等。
EU GMP的要求:
4.31 Logbooks should be kept for major or critical analytical testing, production equipment, and areas where product has been processed. They should be used to record in chronological order, as appropriate, any use of the area, equipment/method, calibrations, maintenance, cleaning or repair operations, including the dates and identity of people who carried these operations out. |
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