obesity
发表于 2025-3-21 16:39:54
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neutrophils
发表于 2025-3-22 00:10:45
The Notified Body: The Conformity Assessment Body for Medical Devices in Europe,ter, we present in detail what a Notified Body is in the sense of the aforementioned regulations and what special requirements are placed on designated notified bodies. We describe when a Notified Body is required for CE marking and what the main tasks of a Notified Body are in the conformity assess
前奏曲
发表于 2025-3-22 01:24:29
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Evolve
发表于 2025-3-22 07:41:03
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渐强
发表于 2025-3-22 10:17:40
Safety Requirements for Medical Devices in Compliance with European Standards,es to comply with the state of the art and how it can be achieved. It also provides a brief overview of the safety requirements of the medical device regulations, with a focus on single fault conditions and the philosophy of integrated safety, together with an attempt to identify possible ways of pr
吹牛需要艺术
发表于 2025-3-22 13:25:21
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都相信我的话
发表于 2025-3-22 18:49:34
Risk Management for Medical Devices in Compliance with EN ISO 14971,its implementation is outlined. In addition, the individual elements of the risk management process are described and discussed in detail. All documents that are considered as evidence of the establishment of a complete risk management process are presented, and their necessary content is shown. The
粗鲁性质
发表于 2025-3-22 21:24:31
Medical Products: Packing and Labeling Requirements, practice. Other legislation, such as CLP and transport of hazardous materials, may apply and have to be considered as well. It has further become common practice that the manufacturer will consider providing information on safe or environmentally responsible disposal of packaging.
Scintillations
发表于 2025-3-23 02:22:06
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微枝末节
发表于 2025-3-23 08:31:50
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