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The 7th DIA China Annual Meeting

Session 0102 Future Direction of Global Drug Development With ICH E17 Guideline Focusing on MRCTs

Session Chair(s)

Yoshiaki  Uyama, PhD

Yoshiaki Uyama, PhD

  • Director, Office of Medical Informatics and Epidemiology
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

General principles on planningdesigning Multi-Regional Clinical Trials E17


Lih-Jiuan  Hsu

Impacts of E17 Guideline for Drug Review and Approval in Taiwan

Lih-Jiuan Hsu

  • Director, Center of Consultation
  • Center for Drug Evaluation, Taiwan
Patrick  Brady, PharmD

Global Drug Development Impact of ICH E17 Guideline_An Industry Perspective

Patrick Brady, PharmD

  • Vice President, Regulatory Affairs Head, Regulatory Policy and Intelligence
  • Bayer AG Pharmaceuticals, Germany

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