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news Ya-Wei - General | 2018-11-08 | Count:3494

Education and training in December 2018

 

2018/12/01  14:00-16:00  The application of clinical trial and human research protection resources- Part 12

14:00-16:00  IRB Review points in human research and study for human protection

 

2018/12/05  16:00-18:00  The clinical research and human protection training for Resident- Part 12

16:00-18:00  Introduction clinical trial spirit and human research protection ethics

 

2018/12/08  13:00-17:00  GCP and IRB training in medicine and medical device clinical trial

13:10-14:00  Introduction ethic and sprit of medicine and medical device clinical trial and DSMP & DSMB

14:00-14:50  The personal responsibility and professional development of Pharmaceutical company/SMO/CRO/CRC/PI/CRA/SC/PM for medicine and medical device clinical trial

15:10-16:00  Introduction regulation and management in medicine and medical device clinical trial

16:00-16:50  SAE/SUSAR/AE/UP/NC in medicine and medical device clinical trial and case discussions

 

2018/12/12  16:00-18:00  The clinical research and human protection training for Resident- Part 9

16:00-18:00  Innovation research on basic and clinical medical science in future

 

2018/12/14  12:00-14:00  The database application of human research and academic ethics- Part 12

12:00-14:00  Introduction PubMed database for human clinical research and academic ethics key points

 

2018/12/15  13:00-17:00  GCP and IRB training

13:10-14:00  GCP and operation of multicenter trial

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

15:10-16:00  Government regulations and legal norms of IRB review standard and experience sharing

16:00-16:50  The conflict of interesting and clinical trial contract

 

2018/12/22  13:00-17:00  GCP and IRB training in genetic research and cell therapy trial

13:10-14:50  Government regulations and legal norms for gene and cell therapy research at protection of participant rights

15:10-16:00  GCP and clinical care management of gene therapy drug (included side effect, SAE, AE and SUSAR reporting)

16:00-16:50  IRB review key points in genetic research and cell therapy trial

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