Description

该平台主要用于按照GMP要求对整个药品生产、检验、审核、放行进行记录、追溯。药品生产记录由操作人员上传、填写后,交由生产负责人审核,生产负责人审核无误后递交请检需求。检验人员得到请检请求后,进行取样、分析,并填写检验报告,交由其他分析人员或者具有分析证书的质量受权人进行复核,复核无误后质量受权人进行产品的放行审核,确认无误后进行放行审批。产品放行后,分析员才可以进行检测报告的打印。

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ALMORS FAQ

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  • How much does ALMORS cost?

    ALMORS is free.

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App Info

Category
Utilities
Languages
English
Recent release
1.4.2 (1 year ago )
Released on
Nov 28, 2018 (6 years ago )
Last Updated
1 week ago
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