| 公司的控股子公司寧波雙成藥業有限公司（以下簡稱“寧波雙成”）於2023年10月30日至2023年11月3日接受了美國食品藥品監督管理局（以下簡稱“FDA”）的藥品批準前現場檢查 ，雙成藥業1月25日公告， 寧波雙成於近日收到美國FDA的通知，寧波雙成作為代加工生產場地。本次CGMP（現行藥品光算谷歌seo光算谷歌广告生產質量管理規範）檢查涉及口服固體製劑，寧波雙成口服固體製劑生產質量管理體係符合美國FDA的CGMP要求。美國FDA確認該檢查已結束，並提供本次現場檢查報告（EIR）。（文章光光算谷歌seo算谷歌广告來源：界麵新聞）產品代號HQ0056，該產品持有人為上海則正生物醫藥股份有限公司 ，該通知和檢查報告已明確寧波雙成通過了此次美國FDA CGMP檢查， |
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