The Role of Data and Safety Monitoring Boards in Human Subjects ResearchJanuary 13, 2018
Target Audience:
This course is designed for Translational Medicine Researchers, Clinical Research Coordinators, Physicians, Allied Health Professionals, Basic Science Researchers, Nurses.
At the end of this activity participants will be able to
- Explain the overall purpose of a data safety monitoring board (DSMB) and how it is formed.
- Recognize the types of clinical trials that are recommended to have DSMB monitoring
- Distinguish between the roles of IRBs and DSMBs
- Identify the main elements of a DSMP
- Discuss the reporting process of adverse and unanticipated events in relation to DSMB responsibilities
- Illustrate statistical procedures in preparing interim efficacy and safety data reports
- Recognise challenges to clinical trials in different environments.
Please register below. Kindly note that we reserve 30 seats for WCM-Q Faculty and Staff on a first come first serve basis.
Your RSVP will be confirmed via email.
Kind Regards,
The Research Division