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Session Chair(s)
Yoshiaki Uyama, PHD, MS, RPH
Associate Executive Director
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Speaker(s)
Impacts of E17 Guideline for Drug Review and Approval in Taiwan
Lih-Jiuan Hsu
Center for Drug Evaluation, Taiwan, Taiwan
Deputy Executive Director
Global Drug Development Impact of ICH E17 Guideline_An Industry Perspective
Patrick Brady, PHARMD
IQVIA, United States
Global Head, Therapeutic Innovation & Regulatory Science
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