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发表于 2019-1-29 13:44:29
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实际上,纵观欧美关于偏差的指南,相关联的往往用事件(event)这个词。有些event是偏差,对质量没有影响或者不涉及SOP的event可以归于incident。
One-off minor discrepancies are usually not formally considered deficiencies,but are brought to the attention of the manufacturer as comments. 参见 PIC/S GUIDANCE ON CLASSIFICATION OF GMP DEFICIENCIES
WHO 指南有个决策树, the event may be considered an Incident(irrelevant event, not impacting product′s quality). It nevertheless needs to be documented (e.g.:recorded in batch record or logbook, as appropriate) in case it needs to be retrieved later as part of an investigation as applicable.
总之,首先企业应当建立自己的SOP,明确定偏差和事件的范围,以及相对应的处理措施。这样才能够很好的执行。 |
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