第一場次：
1. 我國藥品臨床試驗法規現況簡介 (Introduction of Current Regulation for Pharmaceutical Clinical Trials in Taiwan)
黃玫甄副研究員 (衛生福利部食品藥物管理署) Mei-Chen Huang, Associate Researcher, Division of Medicinal Products , Food and Drug Administration, Ministry of Health and Welfare, Taiwan.
2.臺北榮總受試者保護計畫 （The human research protection program of Taipei Veterans General Hospital）
鍾芷萍 醫師 臺北榮民總醫院 神經醫學中心腦血管科 / 臨床研究受試者保護中心 副執行秘書 Dr. Chih-Ping Chung，Division of Cerebrovascular Diseases, Neurological Institute, Deputy Executive Secretary, Human Research Protection Center, Taipei Veterans General HospitalDivision of Cerebrovascular Diseases, Neurological Institute, Deputy Executive Secretary, Human Research Protection Center, Taipei Veterans General Hospital
第二場次：
1.質性研究: 研究方法與IRB申請 (Qualitative research approach: methodology and IRB submission)
穆佩芬 教授 國立陽明大學 護理學院, Professor Pei-Fan Mu, Institute of Clinical Nursing, National Yang-Ming University
2. 質性研究關注的研究倫理議題 (Ethical issues for qualitative research)
穆佩芬 教授 國立陽明大學 護理學院, Professor Pei-Fan Mu, Institute of Clinical Nursing, National Yang-Ming University
最後更新：