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发表于 2021-8-9 19:03:45 | 显示全部楼层 |阅读模式
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发表于 2021-9-28 19:44:25 | 显示全部楼层

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ISO Standardization Is A Key To The Development Of Your Business

Part 2-8 - Medical Electrical Equipment: Specific Safety Requirements And Essential Performance In X-Ray Therapy Equipment Operating Within The Voltage Range From 10 Kv To 1 Mv. En 60601-2-8:2015
Documents that are not specifically defined sometimes are neglected with companies due to various reasons. One reason is the constantly changing characteristics of the standards. EN 60601-2-8.2015 is an important document for businesses dealing with medical equipment. It establishes the essential safety requirements and performance specifications for medical X-ray therapy equipment, which has nominal Xray tube voltages ranging from 10 kV and 1 MV when it is connected to an alternating current mains supply. It includes requirements for reliability and accuracy, which are directly related to the quality of radiation. The 2nd edition replaces IEC 60601-2-8. This edition is a technical update that brings this standard in line the third edition IEC 60061-1-1 and its collateral specifications. We strongly recommend to follow the link to the website for your company if you operate in the area of the mentioned equipment. See the top rated clc catalog standards en-60068-3-8-2003 site.

Innovation Management - Fundamentals & Vocabulary (Iso 56000:2020). EN ISO 56000:2021
For technical standards like, for example, describing the issue of information security, explanatory documents are created to prevent confusion about this or that term. EN ISO 56000: 2021 is one such example. This document gives the basics, concepts, and principles for innovation management and the systematic way to implement it. It can be used to:A) Organizations that implement an innovation management strategy or conduct assessments of innovation management.b. Companies that need to enhance their management of innovative actionsc) customers, users and other interested parties (e.g. Suppliers, partners and funding organizations, investors as also public officials and universities) who wish to be confident in the capabilities of the organization's innovators.d. organizations and other people who are interested in improve communication through an understanding of the terminology that is used in innovation administratione) Providers for training in assessments, training, or consultation regarding the management of innovation and its methods.F. The developers of innovation management standards and other related standards1.2 The document is intended to be applicable to: a) any type of organization regardless of their the type, sector, maturity level or size;b. All kinds of innovations, e.g. product, service, process models and methods all types of innovations, from incremental to radical.C) all types of approaches, e.g. c) All kinds of approaches, e.g., internal and external innovation, market-based design- and technology-driven developments.This document defines the terms and definitions that are applicable to all ISO/TC 279.-developed standards for innovation management and management systems.There are numerous clarifying aspects within this standard. We suggest that you carefully study them and evaluate them against the technological foundation of your company to ensure that the document will be able to enable you to take your organization to the highest possible level. Check out the most popular sist catalog standards sist-en-15250-2007 site.

The Characterisation Of Bulk Materials - Determination Of A Size-Weighted Fine Fraction And Crystallized Silica Content - Part 2 Method For Calculation EN 17289-2:2020
One component of the same standard can complement the other or regulate entirely different sectors. EN 17289-2,2020 is the second section of the standard that was previously in force.This document describes how bulk materials can be calculated to determine the size-weighted portion of fine silica (SWFFF) as well as the fine fraction of size-weighted crystal silica (SWFFCS). The document also defines the preconditions and assumptions that must be met for this method to be valid.This document will enable users to assess bulk materials based on their fine fraction size and the content of crystal silica.A specific method of assessment of the SWFF for diatomaceous earth bulk materials can be found in Annex A. Annex A gives an illustration of how to assess the SWFF of diatomaceous stone bulk materials.This document applies to the bulk materials containing crystalline silicona that have been thoroughly studied and validated to evaluate the size-weighted fine fraction as well as crystalsilica.You can get a better impression of the importance of these standards by comparing the technical parameters of production standards with those of the individual standards. If you have any concerns about the process of implementing this stage, you can get help from experts in the field of international standards. See the top rated iso catalog standards iso-iec-dis-23093-2 information.

Systems And Software Engineering. Software Product Quality Requirements Evaluations And Evaluations (Square) For Software Products. Common Industry Format (Cif) To Ensure Usability User Specifications (Iso 25065.2019). EN ISO 25065:2020
The quality of software is now the most crucial factor in ensuring a position of leadership on international markets. There are specific rules for these markets that must be followed currently. These standards are contained in documents such as EN ISO 25065 2020.This document provides a uniform framework and terminology for defining the requirements of users. It specifies the common industry format (CIF) for a user requirement specification including the content elements and the format to express the requirements.A user requirements specification describes the formal documentation and requirements of the set. It can be utilized to aid in the creation, evaluation, and maintenance of interactive software that is usable.The definition of user requirements is (a) the requirements for user interaction with the system in order to get the desired results (including requirements on system outputs, attributes and their attributes) and; b) the specifications of quality related to use that specify the quality requirements for the outcomes of interactions between users and interactive systems . They can also be utilized to assess the system's acceptance.ISO/IEC 25030 specifies quality requirements. One kind of quality requirements is the use-related quality requirements. The information contained in a requirements specification can be used in documentation resulting from activities in ISO 9241-210 or in human-centered design methods like those in ISO 92421-220.This document is designed to be used by requirements engineers as well as product managers, business analysts and owners of products and others acquiring systems through third parties. CIF's standards cover information related to usability (as specified in ISO 9241-11 and ISO/IEC TR25060).Beyond usability, user requirements can include other perspectives including human-centric quality that was introduced in ISO 9241-220, and other quality-related perspectives that are presented in ISO/IEC 25010and ISO/IEC TS 25011 and ISO/IEC 25030.This document was created to be used in conjunction with interactive systems. However, it could also be used in other areas. The document is not a guideline for any kind of method, lifecycle or process. The elements that constitute the user requirements specification may be utilized for iterative development that includes the development and refinement of requirements (e.g. as in agile development).
Use of this international standard can significantly help your professional work. It can also help you structure your existing process and give you the opportunity to expand your business into new markets and grow your business. Check out the top rated cen catalog standards en-12721-2009a1-2013 blog.

Health Informatics Interoperability Between Devices - Part 20701: Point-Of-Care Medical Device Communications - Service-Oriented Medical Device Exchange Architecture And Protocol Binding (Iso/Ieee 11073-20701:2020) EN ISO 11073-20701:2020
These technologies are not only utilized in the areas which fall under the umbrella of this category but as well in the medical industry. Because the introduction of multiple instruments in medicine is often complex and requires the restructuring of existing systems, international documents are being developed to assist in these processes.
This standard's scope is a service-oriented device architecture and communication protocol specifications for distributed system of Point-of-Care (PoC) medical devices and medical IT systems that require to exchange information or control networked PoC medical devices. It specifies the functional components as well as the communication relations and binding to protocols specifications.This document has a narrow outline and is highly special. It is therefore advised that you study the technical aspects of this document more thoroughly and that, if in doubt you seek out people who have experience selecting international documents. Have a look at the top sist catalog standards sist-en-iso-13585-2012 site.

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