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China Drug Master File (DMF) Registration: A Snapshot on Pathways and Requirements

This is the first article in a series focusing on China […]

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Provisions for Administration of Drug-related Associated Review & Approval for APIs, Excipients. and Packaging Materials (2020 Draft for Comments)

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    Announcement on Issues Concerning the Further Improvement of Drug-related Associated Review & Approval and Supervision (2019 No.56)

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      Announcement for Adjusting Evaluation and Approval for APls, Excipients and Packaging Materials (2017 No.146)

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        Provisions for Drug Registration (2020 No.27)

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