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瀏覽器自帶分享功能也很好用哦~In accordance with the Announcement of the State Drug Administration on Matters Relating to Further Improvement of Drug-Related Review, Approval and Supervision (No. 56 of 2019), it provides enterprises with services relating to the registration of pharmaceutical packages I. The registration of pharmaceutical packages I is a service of the State Food and Drug Administration.
我們的服務：
（1） 藥包材登記I法規(guī)咨詢服務
（2） 藥包材登記I資料撰寫服務
（3） 藥包材登記I質量標準服務
（4） 藥包材登記I批檢驗服務
（5） 藥包材登記I自身穩(wěn)定性研究服務
（6） 藥包材登記I相容性與安全性服務
（7） 藥包材登記I資料遞交CDE及解決發(fā)補問題服務
我們的優(yōu)勢：
（1） 擁有專業(yè)的藥包材登記I法規(guī)、合規(guī)、質量控制團隊
（2） 擁有藥包材登記I資料撰寫團隊
（3） 擁有專業(yè)的質量標準撰寫團隊
（4） 擁有藥包材檢測的CMA、CNAS資質
（5） 擁有專業(yè)的藥包材批檢驗、穩(wěn)定性研究、相容性研究技術團隊
（6） 多種產品成功登記I案例
Our services:
(1) Pharmaceutical package registration I regulatory consulting services
(2) Pharmaceutical package registration I data writing services
(3) Pharmaceutical package registration I quality standard services
(4) Pharmaceutical package registration I batch testing services
(5) Pharmaceutical package registration I self-stability study services
(6) Pharmaceutical package registration I compatibility and safety services
(7) Pharmaceutical package registration I data submission CDE and solve the problem of issuance of replacement services
Our advantages:
(1) Professional regulatory, compliance and quality control team for registration of pharmaceutical package inserts.
(2) We have a team of professional writers for the registration of pharmaceutical packages.
(3) Professional quality standard writing team
(4) With CMA and CNAS qualification for the testing of pharmaceutical packages
(5) Professional technical team for batch testing, stability study and compatibility study of pharmaceutical packaging materials.
(6) Successful registration cases of many products
In accordance with the Announcement of the State Drug Administration on Matters Relating to Further Improvement of Drug-Related Review, Approval and Supervision (No. 56 of 2019), it provides enterprises with services relating to the registration of pharmaceutical packages I. The registration of pharmaceutical packages I is a service of the State Food and Drug Administration.
我們的服務：
（1） 藥包材登記I法規(guī)咨詢服務
（2） 藥包材登記I資料撰寫服務
（3） 藥包材登記I質量標準服務
（4） 藥包材登記I批檢驗服務
（5） 藥包材登記I自身穩(wěn)定性研究服務
（6） 藥包材登記I相容性與安全性服務
（7） 藥包材登記I資料遞交CDE及解決發(fā)補問題服務
我們的優(yōu)勢：
（1） 擁有專業(yè)的藥包材登記I法規(guī)、合規(guī)、質量控制團隊
（2） 擁有藥包材登記I資料撰寫團隊
（3） 擁有專業(yè)的質量標準撰寫團隊
（4） 擁有藥包材檢測的CMA、CNAS資質
（5） 擁有專業(yè)的藥包材批檢驗、穩(wěn)定性研究、相容性研究技術團隊
（6） 多種產品成功登記I案例
Our services:
(1) Pharmaceutical package registration I regulatory consulting services
(2) Pharmaceutical package registration I data writing services
(3) Pharmaceutical package registration I quality standard services
(4) Pharmaceutical package registration I batch testing services
(5) Pharmaceutical package registration I self-stability study services
(6) Pharmaceutical package registration I compatibility and safety services
(7) Pharmaceutical package registration I data submission CDE and solve the problem of issuance of replacement services
Our advantages:
(1) Professional regulatory, compliance and quality control team for registration of pharmaceutical package inserts.
(2) We have a team of professional writers for the registration of pharmaceutical packages.
(3) Professional quality standard writing team
(4) With CMA and CNAS qualification for the testing of pharmaceutical packages
(5) Professional technical team for batch testing, stability study and compatibility study of pharmaceutical packaging materials.
(6) Successful registration cases of many products
滬ICP備2022003614號-1
