Education and training in June 2017

2017/06/03  14:00-16:00  The application of clinical trial and human research protection resources- Part 6

14:00-16:00  To specify in detail and explain skill of Informed Consent Form for clinical trial

2017/06/10  13:00-17:00  The advanced class of GCP and human research protection of participant rights

13:10-14:00  The conflict of interesting and risk assessment at clinical trial

14:00-14:50  Clinical Trial Capacity and New Drug Review Related to Multi-Regional Clinical Trials (MRCT) in Taiwan

15:10-16:00  The human protection and defect occur frequently in clinical trial

16:00-16:50  PI how to team management and distributed responsibility for clinical research

2017/06/13  16:00-18:00  2017 The clinical research training for Resident- Part 6

16:00-18:00  How to write case report and research design

2017/06/17  13:00-17:00  Execution and management of clinical trial and human research protection of participant rights

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 research resources and coordinate of clinical trial

16:00-16:50  The service etiquette of human subject protection for clinical trial and team communication skills

2017/06/24  13:00-17:00  Monitor and Auditor training of clinical trial- Part 1

13:10-14:00  The team management and distributed responsibility requirement in global clinical trial research for PI and study nurse

14:00-14:50  Function and operation of contract research organization and study site

15:10-16:00  Clinical trial inspection regulations

16:00-16:50  Introduction monitor, audit and inspection of clinical trial and case discussion sharing