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太美医疗科技助力安领科生物完成FDA Gateway联调测试 加强药物警戒 ...
指南规定: 2026 年 4 月 1 日之后,IND申请必须向 FDA 的不良事件报告系统(FAERS)提交满足E2B R3规范的SUSAR报告。目前,这些报告使用 PDF 文件以电子 ...
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