Education and training in July 2016

2016/07/04  10:00-12:00  Auditor training for human research and clinical trial   

10:00-12:00  Auditor training for human research and clinical trial

2016/07/05  14:00-16:00  The PI, researcher and study nurse on job training for human research and clinical trial- Part 3

14:00-16:00  The service etiquette of human subject protection for clinical trial and team communication skills

2016/07/07  12:30-13:30  Introduction TMU clinical study database and registration system

12:30-13:30  Introduction TMU clinical study database and registration system

2016/07/09  14:00-16:30  The application of clinical trial and human research protection resources- Part 7       

14:00-16:30  Audit and defect occur frequently for TMUH research

2016/07/12  14:00-16:00  The PI, researcher and study nurse on job training for human research and clinical trial- Part 4   

14:00-16:00  Standard operating procedures writing and design

2016/07/16  13:00-17:00  Inspection new knowledge for human research and clinical trial

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

14:00-14:50  AAHRPP accreditation and human research protection

15:10-16:00  Introduction of international GCP inspection

16:00-16:50  The defect occurs frequently in clinical trial inspection and illustrated to be desired

2016/07/23  13:00-17:00  PI training of human clinical trial- Part 1   

13:10-14:00  Investigator site selection of clinical trial and experience sharing

14:00-14:50  Clinical trial site start up and experience sharing

15:10-16:00  IRB review points and defect occur frequently for research

16:00-16:50  Introduction International Clinical Trials Registry Platform (ICTRP)

2016/07/26  14:00-16:00   Data management method and quality improvement of the trials for HRPP- session first

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

2016/07/28  08:30-10:30  Data management method and quality improvement of the trials for HRPP- session second   

08:30-10:30  Data management method and quality improvement of the trials for HRPP- session second

2016/07/30  13:00-17:00  PI training of human clinical trial- Part 2    

13:10-14:00  The main points of IRB reviewing on genetic and biomarker-related clinical trial

14:00-14:50  The conflict of interesting, Risk Assessment and human protection of clinical trial

15:10-16:00  Clinical trial regulations and cases discussion sharing

16:00-16:50  Personal Information Protection Act and human protection of subject at big data research