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瀏覽器自帶分享功能也很好用哦~《已上市化學藥品藥學變更研究技術指導原則（試行）》、《已上市生物制品藥學變更研究技術指導原則（試行）》、《已上市中藥藥學變更研究技術指導原則（試行）》、協助企業通過研究滿足制劑與藥包材的關聯審評審批要求，使藥包材登記I狀態轉為A狀態。
According to “M4Q(R1): General Technical Document for Registration of Human Drugs”,Technical Guidelines for Pharmaceutical Change Studies of Listed Chemical Drugs (Trial Implementation), Technical Guidelines for Pharmaceutical Change Studies of Listed Biological Products (Trial Implementation), Technical Guidelines for Pharmaceutical Change Studies of Listed Traditional Chinese Medicines (Trial Implementation), and assisting enterprises to meet the requirements for review and approval of the association between preparations and packaged medicines through the study, so as to enable the packaged medicines to be registered in the I status to the A s
我們的服務：
（1） 藥包材登記I轉A的相容性研究服務
（2） 藥包材登記I轉A的密封性研究服務
（3） 藥包材變更研究內容服務
（4） 協助藥包材企業與制劑企業關聯服務
我們的優勢：
（1） 擁有專業的藥包材法規、合規、質量控制團隊
（2） 擁有藥包材登記I轉A的項目研究團隊
（3） 擁有藥包材檢測的CMA、CNAS資質
（4） 擁有專業的藥包材相容性、密封性研究技術團隊
（5） 多種產品關聯A的案例
Our services:
(1) Compatibility study services for registration of I to A in pharmaceutical packages
(2) Sealability study service for I to A registration of pharmaceutical packages
(3) Services for the change of research content of pharmaceutical package materials
(4) Assisting pharmaceutical package material enterprises to associate with preparation enterprises.
Our Advantages:
(1) We have a professional team for regulations, compliance and quality control of pharmaceutical packages.
(2) Have a research team for the project of I to A registration of pharmaceutical package materials
(3) With CMA and CNAS qualification for testing of pharmaceutical packaged goods
(4) Professional research team for compatibility and sealing of pharmaceutical packaging materials.
(5) A variety of products associated with the A case
《已上市化學藥品藥學變更研究技術指導原則（試行）》、《已上市生物制品藥學變更研究技術指導原則（試行）》、《已上市中藥藥學變更研究技術指導原則（試行）》、協助企業通過研究滿足制劑與藥包材的關聯審評審批要求，使藥包材登記I狀態轉為A狀態。
According to “M4Q(R1): General Technical Document for Registration of Human Drugs”,Technical Guidelines for Pharmaceutical Change Studies of Listed Chemical Drugs (Trial Implementation), Technical Guidelines for Pharmaceutical Change Studies of Listed Biological Products (Trial Implementation), Technical Guidelines for Pharmaceutical Change Studies of Listed Traditional Chinese Medicines (Trial Implementation), and assisting enterprises to meet the requirements for review and approval of the association between preparations and packaged medicines through the study, so as to enable the packaged medicines to be registered in the I status to the A s
我們的服務：
（1） 藥包材登記I轉A的相容性研究服務
（2） 藥包材登記I轉A的密封性研究服務
（3） 藥包材變更研究內容服務
（4） 協助藥包材企業與制劑企業關聯服務
我們的優勢：
（1） 擁有專業的藥包材法規、合規、質量控制團隊
（2） 擁有藥包材登記I轉A的項目研究團隊
（3） 擁有藥包材檢測的CMA、CNAS資質
（4） 擁有專業的藥包材相容性、密封性研究技術團隊
（5） 多種產品關聯A的案例
Our services:
(1) Compatibility study services for registration of I to A in pharmaceutical packages
(2) Sealability study service for I to A registration of pharmaceutical packages
(3) Services for the change of research content of pharmaceutical package materials
(4) Assisting pharmaceutical package material enterprises to associate with preparation enterprises.
Our Advantages:
(1) We have a professional team for regulations, compliance and quality control of pharmaceutical packages.
(2) Have a research team for the project of I to A registration of pharmaceutical package materials
(3) With CMA and CNAS qualification for testing of pharmaceutical packaged goods
(4) Professional research team for compatibility and sealing of pharmaceutical packaging materials.
(5) A variety of products associated with the A case
滬ICP備2022003614號-1
