行政院衛生署食品藥物管理局 【發布日期:2013-05-01】 行政院衛生署4家醫療器材代施查核機構,已簽訂「Technical Cooperation Programme on Exchange of Medical Device GMP and ISO 13485 Audit Reports between EU AIMD/MDD/IVDD Notified Body Partners and R.O.C. TFDA Authorized Medical Device GMP Auditing Organizations,Version 2.0」(簡稱臺歐TCP II),雙方同意建立技術合作關係。 詳情請見官網。 |
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