查詢結果
共有 769 筆符合條件的資料
| 序號 | 篇名 | 作者 | 日期 | 期刊 |
|---|---|---|---|---|
| 41 | 精準醫療時代之基因檢測：多基因風險評分（PRS）於臨床應用之倫理與規範考量【本期企劃】 Genetic Testing in the Era of Precision Medicine: Ethical and Regulatory Considerations for the Clinical Application of Polygenic Risk Scores (PRS) |
何之行 | 2025/11 | 月旦醫事法報告 |
| 42 | 病人自主權之損害賠償案：談末期生命照護的為與不為【學習式判解評析】 Dispute on the Infringement of Patient Autonomy in End-of-Life: Discussing What to Do and What Not to Do in End-of-Life Care |
謝宛婷 | 2025/11 | 月旦醫事法報告 |
| 43 | 從代謝疾病到基因世代：新生兒篩檢法律議題之挑戰與台灣展望【本期企劃】 From Metabolic Disorders to the Genomic Era: Legal Challenges of Newborn Screening and the Outlook for Taiwan |
鄒孟珍 | 2025/10 | 月旦醫事法報告 |
| 44 | 歐盟健康資料空間（EHDS）之立法初探：以健康資料二次利用為核心【月旦時論】 The European Health Data Space: Exploring the Secondary Use of Health Data |
何之行 | 2025/10 | 月旦醫事法報告 |
| 45 | 胎兒生命權與婦女生育自主權之衝突及調和——以「嬰兒保護艙」制度為中心【本期企劃】 The Conflict and Reconciliation between Fetal Life and Women's Autonomy—Focus on the “Baby Box” System |
王皇玉 | 2025/10 | 月旦醫事法報告 |
| 46 | 探討生殖醫學公司化之影響【全球瞭望】 Addressing the Consequences of the Corporatization of Reproductive Medicine |
Sara A. Attinger、王郁茜(編譯) | 2025/10 | 月旦醫事法報告 |
| 47 | 體外診斷醫療器材之風險分級與監管架構：以歐盟、美國與台灣為例【本期企劃】 Risk-based Classification and Regulatory Frameworks for In Vitro Diagnostic Devices: A Comparative Study of the EU, the United States, and Taiwan |
呂政諺 | 2025/09 | 月旦醫事法報告 |
| 48 | 醫療前線的把關者：醫事檢驗師的法定執業範圍探索【本期企劃】 Do Right Things at the Right Time: Policy Reflections on Patient Right to Autonomy Act and Hospice in Taiwan |
陳國樟 | 2025/09 | 月旦醫事法報告 |
| 49 | 氣切患者返家之療養指導義務【寰宇醫事裁判】 The Duty of Counselling to the Patients after having Intubation |
黃浥昕(編譯) | 2025/09 | 月旦醫事法報告 |
| 50 | 實驗室開發檢測的監管爭議、訴訟風險與臨床溝通責任【本期企劃】 Navigating the Regulatory Uncertainties, Legal Risks, and Clinical Communication Duties of Laboratory Developed Tests (LDTs) |
黃品欽 | 2025/09 | 月旦醫事法報告 |
