Education and training in November 2017

2017/11/02  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 1

12:00-14:00  How to write research grant proposal of the CDC (Centers for Disease Control, Taiwan) and cooperation with multicenter study and case sharing

2017/11/07  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 2

12:00-14:00  How to write research grant proposal of the MOST (Ministry of Science and Technology) and study case sharing

2017/11/08  12:00-14:00  Quality management and resource application in human research- Part 3

12:00-14:00  The management strategy of human clinical research

2017/11/09  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 3

12:00-14:00  How to write research grant proposal of the MOHW (Ministry of Health and Welfare) and study case sharing

2017/11/10  12:00-14:00  Quality management and resource application in human research- Part 4

12:00-14:00  Introduction Web of Science (SCIE & SSCI) and Journal Citation Reports (JCR) database management system

2017/11/13  12:00-14:00  Quality management and resource application in human research- Part 5

12:00-14:00  The special features and risk assessment in human clinical research

2017/11/15  16:00-18:00  2017 The clinical research training for Resident- Part 11

16:00-18:00  Industry cooperation practice for clinical research and development in future

2017/11/17  12:00-14:00  Quality management and resource application in human research- Part 6

12:00-14:00 Introduction SCOPUS and Science Direct (SDOL) database management system

2017/11/18  14:00-16:00 The application of clinical trial and human research protection resources- Part 11

14:00-16:00  The review points on big data research with common defect and human protection of subject

2017/11/21  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 4

12:00-14:00  How to write research grant proposal of the Government and Industry Cooperation in Practice and study case sharing

2017/11/25  13:00-17:00  The legal ethics and responsibility in human protection for clinical trial team

13:10-14:00  The ethics and spirit in human research investigation for government agencies initiated studies

14:00-14:50  To specify in detail and explain skill of Informed Consent Form at protection of vulnerable groups for clinical trial

15:10-16:50  The responsibility and dispute at legal ethics in human research investigation for government agencies initiated studies

2017/11/27  12:00-14:00  Quality management and resource application in human research- Part 7

12:00-14:00  The ethics and spirit in human research investigation for government agencies initiated studies

2017/11/28  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 5  

12:00-14:00  How to write research grant proposal in the field of Oral Medicine and study case sharing

2017/11/30  12:00-14:00  Writing study trial protocol training and human research protection resources- Part 6

12:00-14:00  How to write research grant proposal an application for new staff and study case sharing