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- Medical deviCE supplier audit checklistatory requirement for a medical deviCE manufacturer, and it is foundation ...2024-09-19 17:27:12
- e agent for medical deviCE in China?...till do not have their own Export LiCEnse, on the other hand, there are NO...2024-09-19 13:53:09
- g Agent for medical deviCE...roblems you meet in the medical deviCE sourcing, and more. Sourcing agents...2024-09-19 13:51:41
- Sourcing medical deviCE in ChinaChina has become the manufacturing CEnter of the world for medical deviCEs, However, searching for a qualifie...2024-09-19 13:40:58
- Ways to find medical deviCE supplier in Chinan search of a qualified medical deviCE supplier, a comprehensive evaluatio...2024-09-19 13:27:46
- Supplier Management for Medical DeviCE CompaniesAs a manufacturer of medical deviCEs, it is your responsibility to be on top of the entire system that sees...2024-09-19 11:46:00
- 欧盟MDD/MDR CE证书过期了，还能用来进行MHRA注册吗？渡安排已获修订，在符合若干条件的情况下，延长欧盟MDD和欧盟AIMDD CE证书的有效期。 以前，证书将一直有效到证书上标明的期限结束，任何剩余的证...2024-07-01 11:50:59
- 如何撰写CE临床评价报告如何撰写CE临床评价报告1既然临床评价报告是临床评价的最后一个阶段，其目的自然不言而喻，这份报告就是要记录整个临床评价过程及其输出。因为，临床评价报告最终会...2019-08-11 12:22:18
- 去哪搜索CE临床评价资料？ 临床数据的定义是什么？CE临床评价指南文件MEDDEV 2.7.1第四版对其定义是：从器械的临床使用中产生的安全、有效信息。具体来说，临床评价中使用的临床数据主要来源于两...2019-06-29 09:52:42
- 怎么撰写CE临床评价报告？临床评价报告（Clinical Evaluation Report，CER）作为产品CE技术文件中的重要文档之一，是证明产品临床使用安全有效的有力佐证。那么，厂商如何能够编写一份完整、详实、清晰的临床评价报告呢？今天...2019-06-23 20:36:18