诺泰生物(688076.SH)通过药品GMP符合性检查

智通财经08-16

智通财经APP讯，诺泰生物(688076.SH)公告，公司于近日收到江苏省药品监督管理局签发的《出口欧盟原料药证明文件》(编号：JS240048)、《药品GMP符合性检查告知书》(苏药监药生告知[2024]231号、232号)，公司连云港工厂的106车间原料药(利拉鲁肽，仅用于出口欧盟文件办理)生产线、106车间原料药(依替巴肽)生产线、101车间原料药(醋酸西曲瑞克)生产线经江苏省药品监督管理局的现场检查，符合《药品生产质量管理规范》要求。

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