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Announcement

Content	Date
Welcome Letter by Dr. Shou Mei Wu, Director General of TFDA	2022-07-19 16:55:15
2022 APEC Good Registration Management (GRM)_Agenda	2022-07-11 16:08:27

All Announcements

Course List

Session 1 Introduction of GRM

Session 2 Planning of Application

Session 3 Preparation of Application Dossier

Session 4 Managing and Conducting the Review

Session 5 Using Facilitated Regulatory Pathways (FRPs) for Special Case Authorizations

Session 6 Communication

Session 7 Topic of Special Interest I: Orphan Drug Regulations

Session 8 Topic of Special Interest II: RWD/RWE for regulatory decision-making