Education and training in November 2015

2015/11/10  12:30-13:30  The global regulations and legal norms of cell med therapy sharing

12:30-13:30  The global regulations and legal norms of cell med therapy sharing

2015/11/14  13:00-17:00  PI training of human clinical trial- Part 1

13:10-14:00  The protocol writing and study design of clinical trial

14:00-14:50  Introduction protocol review information system and application notice

15:10-16:00  Introduction risk management plan for clinical trial drugs

16:00-16:50  The drugs risk management plan case discussion and sharing

2015/11/21  13:00-17:00  PI training of human clinical trial- Part 2

13:10-14:00  Government regulations and legal norms for gene research and protection of subject

14:00-14:50  Checklist of informed consent form assessment and template texts of injury compensation

15:10-16:00  The translational medicine application to Precision Medicine

16:00-16:50  Introduction protocol review points at translational medicine and clinical trial

2015/11/27  12:30-13:30  The basic class of human research and clinical trial- Part 8

12:30-13:30  The clinical trial drugs management (included SAE, AE and SUSAR reporting)

2015/11/28  13:00-17:00  PI training of human clinical trial- Part 3

13:10-14:00  Introduction research resources of library database

14:00-14:50  Introduction database application and references management skill

15:10-16:00  The application of big data, health databank and cloud medical research

16:00-16:50  The cloud research of health database system and government regulations at ethic