Education and training in November 2018

2018/11/01  12:00-14:00  Writing study trial protocol training, legal ethics and human research protection resources- Part 7

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 for legal ethics

2018/11/03  14:00-16:00  Writing study trial protocol training, legal ethics and human research protection resources- Part 8

14:00-16:00  Writing integrated research project skills for project director and study case sharing

2018/11/06  12:00-14:00  The application of clinical trial and human research protection resources- Part 11

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

2018/11/07  16:00-18:00  Writing study trial protocol training, legal ethics and human research protection resources- Part 9

16:00-18:00  The research Blue Ocean Strategy for Traditional Chinese Medicine and Western medicine clinical trial

2018/11/08  12:00-14:00  The clinical research and human protection training for Resident- Part 11

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

2018/11/10  09:00-12:00  Auditor training for medical quality and clinical trial- Part 3

09:00-12:00  Auditor training and case study for joint commission International accreditation (JCIA)：patient safety specification, research ethic responsibility, patient safety report and medical dispute resolution

2018/11/10  14:00-17:00  Writing study trial protocol training, legal ethics and human research protection resources- Part 10

14:00-17:00  Workshop on biomedical database and registration system in clinical study and research ethics - Part 5

2018/11/17  14:00-17:00  Workshop on biomedical database and registration system in clinical study and research ethics - Part 5

14:00-17:00  Introduction evidence-based medicine information resources and how to write an evidence-based clinical review article – Part 6

2018/11/23  12:00-14:00  The database application of human research and academic ethics- Part 11

12:00-14:00  Introduction MicroMedex Drug Reference for human clinical research and academic ethics key points

2018/11/24  09:00-12:00  Auditor training for medical quality and clinical trial- Part 4

09:00-12:00  Auditor training and case study for joint commission International accreditation (JCIA)：GCP specification, research ethics and protection patient safety

2018/11/24  14:00-17:00  Auditor training for medical quality and clinical trial- Part 5

14:00-17:00  Auditor training and case study for Association for the Accreditation of Human Research Protection Programs：DSMP & DSMB, Pharmaceutical company/SMO/CRO/CRC,PI/CRA/SC/PM responsibility and duty in clinical trial audit, clinical trial management and patient safety report (included SAE, AE, SUSAR, UP and NC reporting)