Education and training in August 2016

2016/08/01  14:00-16:00  Data management method and quality improvement of the trials for HRPP- session third

14:00-16:00  Data management method and quality improvement of the trials for HRPP- session third

2016/08/05  14:00-16:00  Data management method and quality improvement of the trials for HRPP-session fourth       

14:00-16:00  Data management method and quality improvement of the trials for HRPP-session fourth

2016/08/06  14:00-16:30  The application of clinical trial and human research protection resources- Part 8       

14:00-16:30  IRB review points and defect occur frequently for research & Introduction International Clinical Trials Registry Platform (ICTRP)

2016/08/12  14:00-16:00  Data management method and quality improvement of the trials for HRPP-session fifth

14:00-16:00  Data management method and quality improvement of the trials for HRPP-session fifth

2016/08/13  13:00-17:00  The basic class of IRB reviewer training  

13:10-14:00  The new medical device laws in Taiwan

14:00-14:50  Introduction unanticipated problem and SAE reporting guideline of clinical trial

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

16:00-16:50  IRB members protocol review points at conflict of interesting, risk assessment and human protection for Research

2016/08/20  13:00-17:00  The advanced class of IRB reviewer training  

13:10-14:00  Receive Informed Consent Form and confirm subjects recruitment interviewee

14:00-14:50  IRB members protocol review points at protection of vulnerable groups for clinical trial

15:10-16:00  Government regulations and legal norms of gene and cell therapy and PI responsibility- 1

16:00-16:50  Government regulations and legal norms of gene and cell therapy and PI responsibility- 2

2016/08/25  08:30-10:30  Auditor training for human research and clinical trial   

08:30-10:30  Auditor training for human research and clinical trial

2016/08/27  13:00-17:00  The professional class of IRB reviewer training     

13:10-14:00  IRB members protocol review points at questionnaire survey research and case discussion

14:00-14:50  IRB members protocol review points at human research and case discussion

15:10-16:00  IRB members protocol review points at clinical trial and case discussion

16:00-16:50  IRB members protocol review points at medical device clinical trial and case discussion

2016/08/29  07:30-08:45  Maintaining Accreditation of AAHRPP for human research protection

07:40-07:50  Maintaining Accreditation of AAHRPP for human research protection and action plan in TMUH

07:50-08:10  Maintaining Accreditation of AAHRPP for human research protection and review points

08:10-08:30  Maintaining Accreditation of AAHRPP for IRB review points and key points to PI