Education and training in December 2016

2016/12/03  14:00-16:30  The application of clinical trial and human research protection resources- Part 12

14:00-16:50  Introduction JIRB review information system and application notice、IRB review points and defect occur frequently for research

2016/12/09  12:00-13:00  Introduction TMU clinical study database and registration system

12:00-13:00  Introduction TMU clinical study database and registration system

2016/12/10  13:00-17:00  IRB and Investigational Device Exemption training- Part 2 

13:10-14:00  GCP explanation of medical device for clinical trial

14:00-14:50  Introduction protocol review application notice form defect occur frequently and suggestion improvement

15:10-16:00  Introduction protocol review key point of medical device clinical trial

16:00-16:50  The protocol review of medical device form defect occur frequently and suggestion improvement

2016/12/17  13:00-17:00  IRB, GCP and Protection of subjects and his right- Part 1

13:10-14:00  Legal responsibility of human research

14:00-14:50  The current situation and dynamic equilibrium for clinical trial contract

15:10-16:00  IRB review standard and experience sharing

16:00-16:50  The conflict of interesting and human protection of GCP

2016/12/24  13:00-17:00  IRB, GCP and Protection of subjects and his right- Part2    

13:10-14:00  Research ethic development and international current situation of IRB review

14:00-14:50  Global perspective of human subject protection and protection of vulnerable groups for clinical trial

15:10-16:00  Introduction IRB ethics, spirit and protection human subject

16:00-16:50  IRB member protocol review points and risk assessment