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  1. 国家药监局关于药品信息化追溯体系建设的指导意见

    《药品信息化追溯体系建设导则》

    《药品追溯码编码要求》

    《药品追溯码标识规范》

    《药品追溯消费者查询结果显示规范》

  2. 《国家药监局 国家卫生健康委 国家医保局 关于做好第三批实施医疗器械唯一标识工作的公告》(2023.02.17)

    《国家药监局 国家卫生健康委 国家医保局 关于做好第二批实施医疗器械唯一标识工作的公告》(2021.09.17)

    《关于深入推进试点做好第一批实施医疗器械唯一标识工作的公告》(2020.09.30)

    《关于做好第一批实施医疗器械唯一标识 工作有关事项的通告》(2019.10.15)

    关于发布《医疗器械唯一标识系统规则》 的公告(2019.07.19)

    医疗器械UDI相关标准规范

  1. Drug Supply Chain Security
    Act (DSCSA)

  2. The Unique Device Identification
    System final rule (UDI Final Rule)

  1. EU-Falsified Medicines Directive

  2. Regulation (EU) 2017/745
    on medical devices

    Regulation (EU) 2017/746
    on in vitro diagnosis medical devices

  1. GS1 Barcoding of
    CONVENTIONAL MEDICINES

  1. Decree of the Government of the Russian Federation of December 14, 2018 No.1556 “On approval of ...

  1. Therapeutic Goods (Medicines—Standard for Serialisation and Data Matrix Codes) (TGO 106) Order 2021

  1. Regulations in the National Medicine
    Control System (SNCM), Law No.13.410

  1. Requirements for Unique Device ldentification (UDI) for Medical Devices

  1. Guidance on Medical Device Unique Device ldentification (UDl) System

  1. Roadmap to the Implementation of GS1 DataMatrix Barcodes on Pharmaceuticals in Canada

  1. Food and Drug Regulatory Agency of the Republic of Indonesia

  1. JFDA New Bar Code Requirements for Pharmaceutical Products on Secondary Packaging