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This workshop will be conducted in Japanese Language only.

Online Registration has been closed. Onsite Registration will be available at Nihonbashi Life Science Building.

Click Here to View the Flyer in Japanese


  • Asami  Ezaki, MS
    Asami Ezaki, MS Division of Strategic Planning and Evaluation & Office of Drug Discovery Support
    Japan Agency for Medical Research and Development, Japan
  • Yasuhiro  Honsho
    Yasuhiro Honsho Associate Director, Safety & Risk Management Department
    Daiichi Sankyo Co., Ltd., Japan
  • Yuji  Ito
    Yuji Ito Prescribing Information Group, RA Functions Dept., Regulatory Affairs Japan
    Novartis Pharma K.K., Japan
  • Kana  Maruyama
    Kana Maruyama Manager, Labeling Group, Regulatory Maintenance Department, RA Division
    Janssen Pharmaceutical K.K., Japan
  • Ken  Nakajima, RPh
    Ken Nakajima, RPh Quality Assurance Division Safety Management Department
    Otsuka Pharmaceutical Factory, Inc, Japan
  • Yuji  Ohne
    Yuji Ohne Pharmacutical Officer, PMS management supervisor, Head of Pharmacovigilance Dept
    SymBio Pharmaceuticals Limited, Japan
  • Keinosuke  Okazaki
    Keinosuke Okazaki Pharmacovigilance, Safety-1
    Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Mikiko  Shitara
    Mikiko Shitara Senior Manager, Regulatory Affairs Dept.
    Alexionpharma GK, Japan
  • Rie  Matsui, RPh
    Rie Matsui, RPh Senior Director, Regional Labeling Head for APAC
    Pfizer R&D Japan, Japan
  • Akiyoshi  Uchiyama
    Akiyoshi Uchiyama President
    Artage Inc., Japan
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Please contact DIA Japan for further information.

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