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发表于 2016-9-30 16:56:32
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继续查法规,看看设备日志的必要性,其中FDA part 211.182 条文中有一条规定:A written record of major equipment cleaning, maintenance (except routine maintenance such as lubrication and adjustments), and use shall be included in individual equipment logs that show the date, time, product, and lot number of each batch processed. If equipment is dedicated to manufacture of one product, then individual equipment logs are not required, provided that lots or batches of such product follow in numerical order and are manufactured in numerical sequence.
基本意思是:关键设备的清洁、维护(日常的简单润滑、调校除外)和使用应包括在该设备的使用日志里,。包括日期、时间、产品和生产批号。如果设备是专用的,只生产一种产品,设备日志是不需要的。
大家看看美国和中国GMP里面规定的不一致。美帝真的抓住设备控制的关键点了。另外,美帝的条文里没有提检测仪器的使用日志,还是另有规定,日后再查。 |
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