00:00:00 01.Opening Remarks
00:22:24 02.20th Anniversary of ICH E5 Bridging Study – Reflection and Future Perspective
00:48:16 03.Policies for ICH E5 and E17 Implementation
01:13:50 04.PMDA’s perspectives on the implementation of ICH E5
01:39:05 05.Critical Visibility: CDE and Its Encounter with Regulatory World
02:06:30 06.Panel Discussion
02:33:07 07.An Overview of Logistics and Analyses of Bridging Study Evaluation Applications
02:59:12 08.Pharmacokinetic Considerations of Bridging Study Evaluation and Cases Studies – Regulatory Perspectives
03:34:00 09.Clinical Considerations of Bridging Study Evaluation and Cases Studies – Regulatory Perspectives
04:10:18 10.Implementation and Considerations of ICH E5 in Asian Regions – Global Pharmaceutical Industry Perspectives
04:25:55 11.Implementation and Considerations of ICH E5 in Asian Regions – Research-based Pharmaceutical Industry Perspectives
04:45:14 12.Panel Discussion
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