Knowledge BASE

显示 17-32 个结果（共 45 个结果）

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  D-723-43 ISO13485:2016 Quality System Requirements For Medical Device

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  D-723-46 Application Of Risk Management To Medical Device Part 1:Concepts & Principles

  $20.00 加入购物车
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  D-723-48 IEC 60601 Safety And Essential Performance Of Medical Electrical Equipment

  $30.00 加入购物车
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  D-723-49 HK Labelling Requirements

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  D-723-50 Process Validation

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  D-723-54 Creating CER Plan And Report – Practical Tips

  $50.00 加入购物车
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  D-723-55 Cleanroom Validation

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  D-723-59 Overview Of Global Medical Device Regulation

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  D-723-60 Application Of Usability Engineering To Medical Device

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  D-723-62 Medical Device AD/Promo Application In Taiwan

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  D-723-63 Product Testing And Regulatory Life Cycle

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  D-723-65 Basic Statistics For Medical Device Registration

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  D-723-66 Device Master Record

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  D-723-67 Post Market Surveillance

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  D-723-68 IEC 62304 Software Validation

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  D-723-69 Cybersecurity

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