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发表于 2017-8-4 17:06:25
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这种情况下,一般风险可控的情况下,实际操作仅仅可以做鉴别的项目+厂家COAD单就可以呢。仅供参考!
201. One comment on 211.80(a) raised several issues relative to the handling of bulk components being held in storage tanks or silos, including the commingling of a new shipment with the remainder from previous shipments and how such lots should be identified. Combining a new bulk shipment of a component in a bulk storage tank with the remainder of a previously received, tested, and approved component lot causes the compositing of the material. The result is that the previously approved material becomes an integral part of an unapproved new lot and cannot be used until such lot is approved for use. However, a manufacturer may choose not to commingle approved lots with unapproved lots of components in bulk storage. In some instances a manufacturer may be able to test components appropriately before introduction to bulk storage as, for example, when a shipment of components is received with a valid certificate of analysis and where identification testing may be sufficient.
选自https://www.fda.gov/downloads/AboutFDA/CentersOffices/CDER/UCM095852.txt
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