Some images has been designed using resources from Unsplash & Pixabay & Pexels & Freepik and some icons from Flaticon
跳到主要內容
:::
教育訓練
:::

112年度臨床研究受試者保護課程(2)-(講義可供下載)

1. 

受試者知情同意的重要性與審查重點

The Importance of Research Participants Informed Consent and IRB Review Focus.

林志翰 組長 

臺北醫學大學/TAIRB秘書長/臺北榮民總醫院AAHRPP認證顧問/IRB(二)委員

Chih-Han Lin

Office of Human Research, Taipei Medical University / Secretary General of TAIRB / Accreditation Consultant for AAHRPP / Member, Institutional Review Board (2),Taipei Veterans General Hospital

 

2. 

PI及研究團隊於研究當中的法律責任與受試者保護

Legal Responsibilities of PI & Research Team in Clinical Research and Subject Protection.

曾育裕 教授

國立臺北護理健康大學通識教育中心教授兼主任/臺灣醫事法學會榮譽理事長/臺北榮民總醫院IRB(一)委員

Yu-Yu Tseng, Professor

Director of General Education Center, National Taipei University of Nursing and Health Sciences / Honorary Chairman of Taiwan Society of Health Law / Member, Institutional Review Board (1),Taipei Veterans General Hospital

 

最後更新:

回到最上