哪里可以做医疗器械CE认证技术文件
TCF文件包括七个方面的内容:
① 简介;
② 产品的规格叙述;
③ 设计之主要档案内容;
④ 风险分析及评估;
⑤ 测试报告及临床诊断资料;
⑥ 文件设计的管制;
⑦ 产品申请的声明宣言。
The TCF file includes seven aspects:
① Introduction;
② Product specification description;
③ The main file contents of the design;
④ Risk analysis and assessment;
⑤ Test report and clinical diagnosis data;
⑥ Control of document design;
⑦ Declaration of product application.
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