Education and training in May 2016

2016/05/06  17:00-18:00  Audit and management quality of human research and clinical trial for HRPP- session second

17:00-18:00  Audit and management quality of human research and clinical trial for HRPP- session second

2106/05/07  14:00-16:30  The application of clinical trial and human research protection resources- Part 5       

14:00-14:50  Big data VS. Clinical trial

15:00-16:30  Introduction current situation and future of Taiwan Biobank and medical development

2016/05/09   14:00-16:00  Auditor on job training for human research and clinical trial    

14:00-16:00  Auditor on job training for human research and clinical trial

2016/05/12  16:00-18:00  Auditor on job training for human research and clinical trial      

16:00-18:00  Auditor on job training for human research and clinical trial

2016/05/14  13:00-17:00  The advanced training for research of clinical trial and human research      

13:10-14:00  The crisis and contingency management of human research and clinical trial

14:00-14:50  Recruitment and Retention of human subjects

15:10-16:00  Government regulations and legal norms of tissue materials research

16:00-16:50  IRB review standard and experience sharing

2016/05/16  12:30-13:30  Audit and management quality of human research and clinical trial for HRPP- session third

12:30-13:30  Audit and management quality of human research and clinical trial for HRPP- session third

2016/05/18  08:00-09:00  Audit and management quality of human research and clinical trial for HRPP- session fourth

08:00-09:00  Audit and management quality of human research and clinical trial for HRPP- session fourth

2016/05/21  13:00-17:00  Biostatistics lesson for Clinical Trials and Research- Part 2

13:10-14:00  Adaptive Design for Clinical Trials

14:00-14:50  New Trends and Controversies in Clinical trial Research

15:10-16:00  Guidance for Industry Non-Inferiority Clinical Trials

16:00-16:50  Statistical Consideration in Non-inferiority Clinical Trials

2016/05/28  13:00-17:00  Monitor and Auditor training of clinical trial- Part 1

13:10-14:00  GCP, audit and monitor for Research quality

14:00-14:50  The PI and auditor's obligation and responsibility in clinical trial

15:10-16:00  The study monitoring and experience sharing

16:00-16:50  Monitoring visit reports and contact reports