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內外醫療器材產品認證註冊申請作業(FDA/TFDA/CFDA/CE) 5.品質系統稽核與文件建立(ISO13485/GMP/QSR) 6.臨床試驗申請規劃與協助執行 7.相關法規、標準、證照申請資料之蒐集/彙整更新及維
GMP
QSR
FDA
1 ~ 1 TWD / month
No management responsibility

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