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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, MS
Director, Office of International Strategy and Planning, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Industry Update
Atsushi Tsukamoto, PhD, MSc
Head is Therapeutic Area Strategies , Daiichi Sankyo, United States
Panelist
Yoshiaki Uyama, PhD, MS, RPh
Associate Executive Director, Regulatory Science Center, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Panelist
Cynthia L. Verst, PharmD, MS
President, R&D Solutions D&DI; 2023 President, IQVIA, United States
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