Program Introduction 課程簡介:
這個課程總共有十二堂課,一堂40 ~ 60分鐘。由兩至三位於藥廠與臨床試驗公司資深臨床試驗專業經理級人員擔任講師,從藥品開發開始講述,並論及藥品優良臨床試驗規範、法規、研究用藥品等基礎臨床試驗知識。希望學員們可以藉由參與這個課程,建立臨床試驗的基本知識,方能再進一步修習臨床試驗協調者(CRC)或臨床試驗監測人員(CRA)等進階課程。
This program consists of 12 courses and one course lasts 40-60 mins. The lecturers are experienced clinical trial professions working in pharmaceutical companies and global CRO, and the program will start from drug development, and include Good Clinical Practice (GCP), Regulations, Investigational Product (IP), and so on. The purpose of this program is to set up the basic knowledge of clinical trials; therefore the participants could further join the advanced program for clinical study coordinator (CRC) and Clinical Research Associate (CRA) program.