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- Register to receive checklists that will help you assess whether you meet the requirements of ISO 13485, Health Canada's CMDCAS program, ISO 9001 and the Medical Device Directive (MDD). 立即注冊,您將收到認證材料單,能夠幫助您評估您是否符合ISO13485、加拿大衛生部的CMDCAS項目、ISO 9001和醫療器械指令(MDD)的要求。
- Medical Device Directive (EU MDD) 藥事法（日本PAL）
- Jinan Tianrui Medical Device Co., Ltd. 濟南天瑞醫療器械有限公司。
- Medical Device Distributing Enterprise License. 醫療器械經(jīng)營(yíng)企業(yè)許可證。
- Medical Device Manufacturing Enterprise License. 醫療器械生產(chǎn)企業(yè)許可證。
- Medical device clinical trials report. 醫療器械臨床試驗報告。
- What's the Scale of China Medical Device Market? 中國醫療器械市場(chǎng)的蛋糕有多大?
- Sterilization :Medical device free of living Microbiology. 無(wú)菌:醫療器具上無(wú)存活微生物。
- Chongqing Chinabase Company - Chris Liu medical device. 中基公司-劉先生醫療器械。
- This paper also cited some common medical device package systems. 本文最后還列舉了常見(jiàn)的醫療器械包裝系統。
- To set up, develop and mange regional Medical device wholesalers and direct customer management (Commercial sales) team. 建立、發(fā)展和管理合格的大區醫療器械經(jīng)銷(xiāo)商及直銷(xiāo)客戶(hù)的管理(商務(wù))團隊。
- Familiar with the supply chain management of Medical Device industry. 熟悉醫療器械供應鏈管理流程。
- Medical device civil suits are preempted, but for how long, and are drugs next? 醫療器械民事訴訟是搶先，但多久，是藥品呢？
- The oxygen tubing conforms to Council Directive MDD/93/42/EEC concerning Medical Devices. 本產(chǎn)品符合歐盟MDD/93/42/EEC指令要求。
- Coordinate with HQ audit and external audit about Medical Device and Drug. 協(xié)調中心審計，醫療器械和藥品相關(guān)的外部審計。
- A special medical device for the treatment of congenital megacolon is designed. 摘要設計一種用于治療先天性巨結腸的專(zhuān)用醫療器材。
- SDA of China is in charge of the monitoring and registration of importing medical device. 負責進(jìn)口醫療器械的注冊和監督工作。
- Responsible for the quality specification of the final medical devices. 負責醫療器械成品的質(zhì)量標準。
- To set up, develop and mange regional Medical device wholesalers management (Commercial sales) team. 建立、發(fā)展和管理合格的大區醫療器械經(jīng)銷(xiāo)商的管理(商務(wù))團隊。
