iPhone Screenshots

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。

What’s New

Version 1.4.2

新增待复核详情驳回功能

App Privacy

The developer, 液化空气(中国)投资有限公司, indicated that the app’s privacy practices may include handling of data as described below. For more information, see the developer’s privacy policy.

Data Not Collected

The developer does not collect any data from this app.

Privacy practices may vary based on, for example, the features you use or your age. Learn More

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