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[V6-S4] HTA in Japan – What Should Pharmaceutical Companies Do?
Session Chair(s)
Kenji Adachi, PhD
Medical Affairs - Health Economics and Outcomes Research, Gilead Sciences, Inc., Japan
Speaker(s)
Clinical Trial Design, Analysis and Reporting Strategies to Maximize Reimbursement Success <Remote Presentation via Internet>
Christine Fletcher, MSc
VP/Head, Speciality and Primary Care Statistics, GlaxoSmithKline, United Kingdom
Patient-Centric Postmarketing Studies on Safety, Effectiveness and Value
Nancy A Dreyer, PhD, MPH, FISPE
Founder, Dreyer Strategies LLC, United States
What Should We Do During Drug Development and Postmarketing When Introducing HTA in Japan?
Kotoba Okuyama
Sr. Biometrician, Biostatistics and Research Decision Sciences, MSD K.K., Japan
TBA
Toshihiko Aranishi, PhD
Research Scientist, Health Outcomes/Health Technology Assessment, Eli Lilly Japan K.K, Japan
Current HTA Discussion for Japan’s Health Care Policy, and Roles of Academia
Takeru Shiroiwa, PhD
Senior Researcher, Department of Health and Welfare Services, National Institute of Public Health, Japan
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