The objectives of the program are:
- To train students to become familiar with the principles, regulations, design, and practice related to clinical trials.
- To equip students with the ability to write and execute clinical trial plans, expand the depth of their research analysis capabilities, and independently complete investigator-initiated clinical trial proposals.
The course content includes a systematic introduction to the International Conference on Harmonisation Guidelines – Good Clinical Practice (ICH-GCP) regulations, Collaborative Institutional Training Initiative (CITI) online certification, clinical trial planning and research methods, statistical methods in clinical trials, proposal format and writing essentials, informed consent forms and procedures, data collection formats, sample trial plans, and IRB application processes. Industry professionals will also share practical operations to enhance students’ understanding of clinical trial practices.
For more details and registration, please see the link below: https://cee.tmu.edu.tw/Course/CourseSingle?courseid=QzExMzAwMDc2
