本課程旨在提昇研究生瞭解健康產業產品開發或評估時可能涉及臨床試驗時的相關規範與法規。課程內容將涵蓋臨床試驗時有關受試者之保護，人體試驗審議會等議題，此外，本課程亦會探討執行時相關實務事項，以使研究生有更正確之認知。

This course is designed to teach student understanding the related regulations of clinical trials that during the development or evaluation of health products. The content of the course include study subject protection and investigational review board issues. The implementation of the clinical trial will also cover in this course. With abovementioned, the student shall have well recognition related to clinical trial.