Overview
How do countries across the globe collaborate effectively in delivering innovative pharmaceutical products, medical devices, and regenerative medical products to patients, in the fastest and most efficient way possible? With healthcare product development becoming increasingly global, the time has come to deepen the discussion on how to leverage the individual strengths of countries, promote better collaboration, and strengthen global partnerships, in order to build the ideal ecosystem for creating medicines, medical devices, and regenerative medical products.
Furthermore, innovative technologies such as artificial intelligence (AI), big data/genomics, and cell/gene therapies are poised to transform healthcare product development across the globe – join us at the DIA Japan Annual Meeting 2018, to discuss these topics and the future of healthcare!
Our two invited keynote speakers will be Professor Guido Rasi, Executive Director of the European Medicines Agency (EMA) and Professor Satoru Miyano of Tokyo University, a leading expert in the fields of genome informatics and AI. On day one of our agenda, our first DIA Japan Annual Meeting innovative DIAmond session will be convened by members of the “Innovation Project” led by The International Coalition of Medicines Regulatory Authorities (ICMRA). Our second DIAmond Session, Innovative Clinical Trials, will be led by top leaders from industry, government, and academia, and share their expert insights into clinical trials of the future in the evolving contexts of innovative technologies and environmental changes. General sessions will address other critical “hot topics,” and the meeting also features our popular PMDA Town Hall Meeting and special chat session.
We look forward to welcoming you at Tokyo Big Sight from November 11-13, 2018 for stimulating discussions around promoting better collaboration to drive global health and innovation in this era of medical and scientific transformation.
We hope to see you there!
Program Committee
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Takuko Sawada • Director of the Board, Executive Vice President
Shionogi & Co., Ltd., Japan -
Kazuhiro Kanmuri, PhD • Vice President, Product Development and Clinical Operations
Ascent Development Services Inc, Japan -
Taro Amagasaki, PhD • Head, Analytics Japan
Novartis Pharma K.K., Japan -
Noriko Fujiwara, MS, RN • Project Researcher, Oncology nurse
IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Japan -
Yoshikata Furuya, MSc • Manager, General Affairs Division
Sankeien Hoshoukai Foundation, Japan -
Shinzo Hiroi, PhD, MPH, RPh, PMP • Head of Global Medical Affairs
Shionogi & Co., Ltd., Japan -
Kazuo Ichikawa, PhD, PMP • yyy
Xxx, Japan -
Katsuhiko Ichimaru • Review Director, Office of New Drug IV
Pharmaceuticals and Medical Devices Agency (PMDA), Japan -
Akiko Ikeda, RPh • Associate Director, Regulatory Development Dept.
Janssen Pharmaceutical K.K., Japan -
Toshiko Ishibashi, PhD, RN • Associate Director,Oncology Medical Science Department
Daiichi Sankyo Company, Limited, Japan -
Kazuhiko Ishida, MSc, RPh • Director, Pharmacovigilance
Astellas Pharma Inc., Japan -
Miyuki Kaneko • Japan Regulatory Portfolio Lead, Regulatory Affairs
Pfizer R&D Japan G.K., Japan -
Yoko Kazami, RPh, PMP • Manager, Research & Development
Nobelpharma Co., Ltd., Japan -
Noriatsu Kono, MPharm • Organizational management
Pharmaceuticals and Medical Devices Agency (PMDA), Japan -
Yukihiro Matsuda, MSc • Senior Manager, Clinical Operations
ICON Japan, Japan -
Yasutsugu Nakano • Senior Director, Regulatory Affairs Department
Shionogi & Co., Ltd., Japan -
Motohide Nishi, MBA • Japan Site Leader & VP Professional Services
Medidata Solutions K.K., Japan -
Minori Niso • Brand Marketing Director, APAC Marketing
Parexel, Japan -
Atsushi Noguchi, MS • Reviewer, Office of New Drug V
Pharmaceuticals and Medical Devices Agency, Japan -
Kimiya Okazaki, PharmD, PhD • Associate Department Manager, Regulatory Intelligence, Regulatory Affairs
GlaxoSmithKline K.K., Japan -
Mikiko Shitara • Senior Manager, Regulatory Affairs Dept.
Alexionpharma GK, Japan -
Kuniko Shoji • Vice-Dean, School of Health Innovation
Kanagawa University of Human Services, Japan -
Keiko Tsumori, MSc • Associate Director, Medical Writing, Regulatory Affairs Area, Japan Development
MSD K.K., Japan -
Tadashi Urashima, PhD • Performance and Digital Analytics Lead, Medical & Development Excellence Japan
GlaxoSmithKline K.K., Japan -
Koichiro Yuji, MD, PhD, FACP • Project Associate Professor, The Institute of Medical Science
Japan -
Junichi Nishino, MSc, RPh • Head, Regulatory Affairs Department
Otsuka Pharmaceutical Co., Ltd., Japan -
Junko Sato, PhD • Director, Office of International Programs
Pharmaceuticals and Medical Devices Agency (PMDA), Japan -
Atsushi Tsukamoto, PhD, MSc • Vice President, New Drug Regulatory Affairs Department
Daiichi Sankyo Company, Limited, Japan
