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news Ya-Wei - General | 2017-08-01 | Count:1109

Education and training in August 2017

 

2017/08/05  The application of clinical trial and human research protection resources- Part 8

14:00-16:00  The conflict of interesting and risk assessment at clinical trial

 

 

2017/08/08  The research team of clinical trial and human research on-the-job training-Part 1 

12:00-14:00 How to do a good clinical trial in human research and experience sharing

 

 

2017/08/10  The research team of clinical trial and human research on-the-job training-Part 2

12:00-12:30  Introduction TMU-eJIRB review information system and application in human clinical research

12:30-13:00  Introduction TMU-biobank review information system and application in human clinical research

13:00-13:30  Introduction TMU- Clinical Trial Management System and application notices

13:30-14:00  Introduction TMU-Human Research Audit System and application notices

 

 

2017/08/12  13:00-17:00  The basic class of GCP and human research protection of participant rights at a new medical device product

13:10-14:00  The global regulations and legal norms of new medical device and future development

14:00-14:50  A new medical device product how to hit the market in USA and EMA

15:10-16:50  Government regulations and legal norms of medical device clinical trial and IRB review points

 

 

2017/08/15  The research team of clinical trial and human research on-the-job training-Part 3

12:00-14:00   Introduction TMU clinical study database and registration system for human clinical research

 

 

2017/08/16  16:00-18:00  2017 The clinical research training for Resident- Part 8

16:00-18:00  Big Healthcare Data Analytics on clinical research

 

 

2017/08/18  The research team of clinical trial and human research on-the-job training-Part 4

12:00-14:00  Introduction research resources and application of library database

 

 

2017/08/19  13:00-17:00  The advanced class of GCP and human research protection of participant rights at a new medical device product

13:10-14:00  Introduction medical device definition and scope in GCP specification for clinical trial

14:00-14:50  The protocol writing and study design of medical device from defect occur frequently and suggestion improvement

15:10-16:00  Statistics and data management in medical device for clinical trial

16:00-16:50  Statistical analyses and audit review points in GCP specification for medical device clinical trial

 

 

2017/08/21  14:00-17:00  Introduction evidence-based medicine information resources and how to write an evidence-based clinical review article – Part 1

14:00-17:00  Introduction evidence-based medicine information resources and how to write an evidence-based clinical review article – Part 1

 

 

20171/08/23  16:00-18:00  2017 The clinical research training for Resident- Part 7

16:00-18:00  The enlightenment of research and medical exploitation for resident

 

 

2017/08/31  12:00-14:00  Auditor on job training for human research and clinical trial-Part 1

12:00-14:00  Auditor training for human research and clinical trial in data management method and quality improvement

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