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

    General Office of the General Administration of the people's Republic of China solicits opinions on the quality management standard for non clinical drug research (Revised Version)

    • Last Update: 2016-08-22
    • Source: Internet
    • Author: User
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    Source: CFDA 2016-8-22 in order to improve the quality of non clinical drug research, the State Food and Drug Administration organized the revision of the quality management specification for non clinical drug research, drafted the quality management specification for non clinical drug research (Revised Draft), and now solicited opinions from the public Please feedback the relevant opinions to the State Food and Drug Administration (drug and cosmetic registration administration department) by email before October 18, 2016 Contact: Jing Shufang email: yjjdc@cfda.gov.cn Annex: drug non clinical research quality management specification (Revised Version) General Office of food and Drug Administration August 17, 2016 Annex: drug non clinical research quality management specification (Revised Version) Doc
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