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Program Committee
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Jun Yamakami, PhD Senior Regulatory Expert, Regulatory Affairs Department Regulatory Consulting
A2 Healthcare Corporation, Japan -
Kazuishi Sekino, MS Director of MID-NET operation and management, Office of Medical Informatics and
Pharmaceuticals and Medical Devices Agency, Japan -
Satoko Utsunomiya Regulatory Affairs Area, Japan Development
MSD K.K., Japan -
Yuko Hata Associate director, Therapeutic Area Regulatory, Japan Regulatory Affairs
Takeda Pharmaceutical Company, Japan -
Toshinori Higashi, PhD Vice President, Regulatory Science
KAKEN PHARMACEUTICAL CO.,LTD., Japan -
Akifumi Kamata, PhD Office of New Drug I
Pharmaceuticals and Medical Devices Agency, Japan -
Miyuki Kaneko Japan Regulatory Portfolio Lead, Regulatory Affairs
Pfizer R&D Japan G.K., Japan -
Yukiko Kato Reviewer, Office of New Drug I
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
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