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Pharmaceuticals and Medical Devices Agency (PMDA) Town Hall
Program Code:
223
Date:
Tuesday, June 25, 2013
Time:
8:00 AM to 9:30 AM
EST
CHAIR
:
Nobumasa Nakashima, PhD (SCHAGY), Director, Office of International Programs, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
SPEAKER
(S):
Takao Yamori, PhD (SPKAGY), Director of Center for Product Evaluation, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Tatsuya Kondo, MD,PhD (SPKAGY), Chief Executive, Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Kazuhiko Mori,
MS (SPKAGY), Managing Director, Kobe Cluster,
Foundation for Biomedical Research and Innovation (FBRI), Japan
Kazuhiko Mori, MS, is currently the Chief Safety Officer of Pharmaceuticals and Medical devices Agency (PMDA). He oversees the post marketing safety measures for pharmaceuticals and medical devices, GMP inspection for pharmaceutical manufactures and QMS inspection for medical devices manufactures.
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Description
PMDA will explain and answer questions from the audience about Japanese regulation, PMDA's current situation, activities and future initiatives for faster and more efficient review to cope with medical products using advanced science technology.