Education and training in July 2017

2017/07/01  The application of clinical trial and human research protection resources- Part 7

14:00-16:00  Artificial Intelligence clinical research in gene big data will redesign healthcare development and future

2017/07/08  13:00-17:00  Monitor and Auditor training of clinical trial- Part 2

13:10-14:00  The clinical trial research requirement, communication and challenge for auditor and study manager

14:00-14:50  Auditor at conflict of interesting, risk assessment and human protection for Research

15:10-16:00  Introduction of FDA and Japan international GCP inspection

16:00-16:50  Introduction of EMA international GCP inspection

2017/07/15  13:00-17:00  Standards of Government Law for The basic class of IRB reviewer training

13:10-14:00  The spirit and ethics in human research and clinical trial

14:00-14:50  Government regulations and legal norms of IRB review standard and experience sharing

15:10-16:50  Clinical trial regulations and cases discussion sharing

2017/07/19  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

2017/07/22  13:00-17:00  The professional class of IRB reviewer training

13:10-14:00  IRB review points at clinical trial protocol and case discussion

14:00-14:50  Receive Informed Consent Form and confirm subjects recruitment interviewee and IRB review points

15:10-16:50  IRB review points in research methods to included questionnaire survey, an interview and existing data system

2017/07/29  13:00-17:00  GCP Specification of a new medical device product

13:10-14:00  GCP explanation of medical device for clinical trial

14:00-14:50  Introduction protocol review application notice form defect occur frequently and suggestion improvement

15:10-16:00  Introduction protocol review key point of medical device clinical trial

16:00-16:50  The protocol review of medical device form defect occur frequently and suggestion improvement