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PMDA Town Hall
Session Chair(s)
Daisuke Tanaka, PhD
Office Director, Office of International Programs
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
PMDA strives and implements various supports to promote regulatory sciences and accelerate product developments based on “4Fs” concept of priorities. In this session, PMDA will share the latest information on its policies and initiatives.
Learning Objective : Recognize latest information on the Pharmaceuticals and Medical Devices Agency’s activity and Japanese regulations in medical products area; Describe how to develop medical products in Japan; Discuss issues on medical products regulation with senior PMDA officials.
Speaker(s)
PMDA Update
Daisuke Koga, MSc, RPh
Ministry of Health, Labour and Welfare (MHLW), Japan
Director, Office of International Regulatory Affairs
Industry Update
Atsushi Tsukamoto, PhD, MSc
Daiichi Sankyo, United States
Head is Therapeutic Area Strategies
Panelist
Yoshiaki Uyama, PhD, RPh
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Associate Executive Director
Panelist
Cynthia L. Verst, PharmD, MS
IQVIA, United States
President, R&D Solutions D&DI; 2023 President
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