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Tokyo Big Sight

Nov 16, 2014 9:00 AM - Nov 18, 2014 6:30 PM

3-11-1 Ariake, Koto-ku, Tokyo, 135-0063 Japan

11th Annual Meeting DIA Japan 2014

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Continuing-Education

Continuing-Education

Short Course or Primer

To keep you at the forefront.

Nov 16, 2014

#10 HTA 2016? What are the challenges for Japan?:

Nov 16, 2014

#1 Basic Introduction for Non-Specialist:

Drug-Drug Interaction and Summary of Change in New Japanese Drug-Drug Interaction Guideline

Nov 16, 2014

#2 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 1:

Nov 16, 2014

#3 Action Learning for Six Sigma Analytical Tools Using Real Case Studies:

Nov 16, 2014

#4 Coaching as a Diverse Communication Tool Across Functions and Areas:

Nov 16, 2014

#5 The Basics of “Investigator Initiated Trial (IIT)” Regulation:

Nov 16, 2014

#6 Prediction for Human Pharmacokinetics and Safety Using Systems Pharmacology:

Nov 16, 2014

#7 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 2:

Nov 16, 2014

#8 An Introduction to Adaptive Designs:

Nov 16, 2014

#10 HTA 2016? What are the challenges for Japan?:

Nov 16, 2014

#1 Basic Introduction for Non-Specialist:

Drug-Drug Interaction and Summary of Change in New Japanese Drug-Drug Interaction Guideline

Nov 16, 2014

#2 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 1:

Nov 16, 2014

#3 Action Learning for Six Sigma Analytical Tools Using Real Case Studies:

Nov 16, 2014

#4 Coaching as a Diverse Communication Tool Across Functions and Areas:

Nov 16, 2014

#5 The Basics of “Investigator Initiated Trial (IIT)” Regulation:

Nov 16, 2014

#6 Prediction for Human Pharmacokinetics and Safety Using Systems Pharmacology:

Nov 16, 2014

#7 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 2:

Nov 16, 2014

#8 An Introduction to Adaptive Designs:

Program Committee

Hiroshi Watanabe, MD, PhD Vice President
Hamamatsu University School of Medicine, Japan
Kenji Nagaya Project Manager, Clinical Research Center
Nagoya Medical Center, Japan
Kasumi Daidoji, PhD, RPh Associate Director, Clinical Planning & Development Dept., Medical Headquarters
Eisai Co., Ltd., Japan
Hideki Hanaoka, MD, PhD
Chiba University Hospital, Japan
Akiko Ikeda, RPh Associate Director, Regulatory Development Dept.
Janssen Pharmaceutical K.K., Japan
Eiji Kajiwara Director, CMC Regulatory Affairs
MSD K.K., Japan
Kazuhiro Kanmuri, PhD Vice President, Product Development and Clinical Operations
Ascent Development Services Inc, Japan
Kazutoshi Maki Chairman
GENEX Partners, Japan
Kana Maruyama Manager, Regulatory Labeling, Regulatory Affairs
Viatris Pharmaceuticals Japan Inc., Japan
Koichi Miyazaki, PhD Senior Director, Group IV, Oncology Clinical Development Department
Daiichi Sankyo Co., Ltd., Japan
Motohide Nishi, MBA Japan Site Leader & VP Professional Services
Medidata Solutions K.K., Japan
Junichi Nishino, MSc, RPh Head, Regulatory Affairs Department
Otsuka Pharmaceutical Co., Ltd., Japan
Masayo Oishi, PhD Clinical Pharmacologist, Clinical Pharmacology, Clinical Research
Pfizer Japan Inc., Japan
Satoshi Saeki, MSc Head of Japan Operational Excellence, Medical Affairs, Japan
Astellas Pharma Inc., Japan
Shuji Sumida, MSc, RPh Senior Director, Quality & Regulatory Compliance Unit
Chugai Pharmaceutical Co., Ltd., Japan
Satoru Tsuchiya, MSc Senior Director, Global Data Design Office
JPMA (Japan Pharmaceutical Manufacturers Association)/Sumitomo Pharma, Co., Ltd., Japan
Naoyuki Yabana, PhD Director, Office of In Vitro Diagnostics
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Takeharu Yamanaka, PhD Professor, Department of Biostatics, School of Medicine
Yokohama City University, Japan
Yoshihiko Ono, RPh Head of Regulatory Affairs
MSD K.K., Japan
Junko Sato, PhD Associate Executive Director
Pharmaceuticals and Medical Devices Agency (PMDA), Japan

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