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   試閱

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

040-053

風險分級、實驗室開發檢測、體外診斷醫療器材、risk-based classification、laboratory developed tests、in vitro diagnostic devices

月旦醫事法報告

202509 (107期)

元照出版公司

10.53106/241553062025090107004  複製DOI  DOI查詢

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