Written in easy-to-understand language that appeals to all learning types, this book simplifies the process of learning hundreds of difficult to pronounce medical terms into manageable steps. Full-color illustrations and an attractive new design make this book inviting and straightforward to use. ...
equal- having the same quantity, value, or measure as another; "on equal terms"; "all men are equal before the law" Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc. Translations --- Select a language: Want to thank...
NOTE3.Intermsoftheinitialconditionofmedicaldevices,medicaldevice manufacturers generally sterilize large numbers of similar medical devices thathavebeenproducedfromvirginmaterial.Healthcarefacilities,onthe other hand, must handle and process both new medical devices and reusable medicaldevicesofdifferentdescription...
General requirements ISO 18113-1:—, In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements EN 980, Symbols for use in the labelling of medical devices 3 术语和定义 对于本标准,GB/T XXXX-1/ISO 18113-1...
【英语版】国际标准 ISO 18113-1:2022 EN In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements 体外诊断医疗器械 制造商提供的信息(标签) 第1部分:术语、定义和一般要求.pdf 关闭预览 想预览更多内容,点击免费...
TCM, a 2,000-year-old practice, is fundamentally different from modern Western medicine in terms of theoretical concepts, such as the model of the body and origin of diseases. TCM has gained increasing public attention after Chinese pharmacist Tu Youyou was awarded the 2015 Nobel Prize in Phys...
ISO14971:2019,Medicaldevices—Applicationofriskmanagementtomedicaldevices ISO14971:2019,医疗器械—风险管理在医疗器械中的应用 3Termsanddefinitions 3术语和定义 Forthepurposesofthisdocument,thetermsanddefinitionsgiveninISO10993-1andthefollowingapply. 就本文件而言,ISO10993-1及以下给出的术语和定义适用。 ISOand...
ISO 18113-1:2022体外诊断医疗器械.制造商提供的信息(标签).第1部分:术语、定义和一般要求 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements首页标准
ISO10993-16,Biologicalevaluationofmedicaldevices—Part16:Toxicokineticstudydesignfordegradation productsandleachables ISO10993-16,医疗器械的生物评价—第16部分:降解产物和可浸出物的毒代动力学研究设计 3Termsanddefinitions 3术语和定义 Forthepurposesofthisdocument,thetermsanddefinitionsgiveninISO10993-1,ISO10993-2...
Further, there are many terms in ISO 13485 unique to medical devices. ISO 13485 also retained the role of a quality representative to top management, where ISO 9001 removed this in many aspects. Interestingly, ISO 9001 has a lot more requirements for monitoring external providers for performance...