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    Home > Active Ingredient News > Drugs Articles > General Office of the General Administration of the people's Republic of China solicits public opinions on the quality management standard for clinical trials of drugs (Revised Version)

    General Office of the General Administration of the people's Republic of China solicits public opinions on the quality management standard for clinical trials of drugs (Revised Version)

    • Last Update: 2016-12-05
    • Source: Internet
    • Author: User
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    Source: CFDA 2016-12-5 in order to improve the quality of drug clinical research, the State Food and Drug Administration revised the quality management specification for drug clinical trials (Order No 3 of the former State Food and Drug Administration), drafted the quality management specification for drug clinical trials (Revised Draft), and now solicited opinions from the public Please send relevant comments to the drug and cosmetic registration department of the State Food and drug administration by email before January 31, 2017 Contact person: Xie xingyong email: xiexy@cfda.gov.cn Annex: drug clinical trial quality management specification (Revised Version) General Office of food and Drug Administration December 1, 2016 Annex: drug clinical trial quality management specification (Revised Version) Docx
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