International Medical Device Regulators Forum logo
A- A+ print this page

Roadmap for implementation of UDI system

This work item is now complete. This page has been retained for historical reference.

This item sought to define the path to implementing a globally harmonized approach to a uniform device identification system, and builds on the earlier work of GHTF.

Working Group Chair: Laurent Selles, Europe. contact Laurent Selles

Working Group Membership: Regulator and stakeholder membership

Canada

    • Thomas Hazle
    • Health Canada

China

    • Liang Yan
    • SFDA
    • JingLi Li
    • SFDA
    • Jun Li
    • SFDA

European Union

    • Matthias Neumann
    • EU Regulatory Authorities

Japan

    • Hiroshi Ishikawa
    • PMDA
    • Yuko Kitayama
    • PDMA
    • Susumu Takahashi
    • PDMA

Korea

    • Hye-Won Roh
    • KFDA
    • Dr Kim
    • KDFA

Singapore

    • Joanna Koh
    • AHWP Regulator
    • Xuefang Liu
    • AHWP Regulators
    • Lindsay Tao
    • AHWP Stakeholder

United States

    • Jay Crowley
    • FDA

AdvaMed

    • Jeff Secunda
    • AdvaMed
    • Jackie Elkin
    • AdvaMed
    • Tom Werthwine
    • AdvaMed

EMDA (IVD)

    • Jesus Rueda
    • EMDA (IVD)

Eucomed Medical Technology

    • Volker Zeinar
    • EUCOMED

Global Diagnostic Imaging, Healthcare IT & Radiation Therapy Trade Association

    • Nicole Denjoy
    • DITTA
    • Tracey Holevas
    • DITTA

JIRA

    • Shigetaka Miura
    • JIRA
    • Tatsuo Heki
    • JIRA
    • Naoki Morooka
    • JIRA