Education and training in December 2017

2017/12/02  The application of clinical trial and human research protection resources- Part 12

14:00-16:00  The improper at clinical research defect occur frequently and research ethics

2017/12/09  13:00-17:00  The team work training for GCP clinical trial and human research

13:10-14:00  The management and conduction in GCP and team communication skills for clinical trial

14:00-14:50  How to improved implementation efficiency and research quality for clinical trial team

15:10-16:50  The responsibility of human researcher and how to improved implementation clinical trial quality depend on legal procedure when researcher to violate the rule

2017/12/16  13:00-17:00  Ethics and regulation of human cell therapy products and accessory protocol writing in clinical trial

13:10-14:50  Introduction regulations and legal norms of human cell med therapy product research and review points

15:10-16:00  The accessory protocol writing of human cell med therapy product research and case sharing

16:00-16:50  The regulations and legal norms of cell med therapy and human cell therapy products accessory protocol writing in clinical trial review points

2017/12/20  16:00-18:00  2017 The clinical research training for Resident- Part 12

16:00-18:00  Introduction JIRB review information system and application notice

2017/12/23  13:00-17:00  Quality management and IRB review ponit in human research and clinical trial

13:10-14:00 The management strategy of human clinical research

14:00-14:50 Introduction monitor and auditor in clinical trial research quality

15:10-16:00 IRB Review points in clinical trial of medical drug and device

16:00-16:50 IRB Review points in human research and study