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发表于 2021-9-2 01:17:35 | 显示全部楼层 |阅读模式
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发表于 2021-9-28 20:29:28 | 显示全部楼层

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ISO Standardization Is Crucial To The Success Of Your Company

Part 2-8 - Electrical Medical Equipment: Specific Requirements For Safety And Vital Performance In Therapeutic X-Ray Equipment Operating Within The Voltage Range Of 10 Kv To 1 Mv. En 60601-2-8:2015
Companies sometimes ignore narrowly defined norms and documents for a variety reasons. The reason for this is the standards are constantly changing. EN 60601-2-8.2015 is recognized as one of the most significant documents for medical equipment businesses. It specifies specific safety and performance requirements that are crucial for the use of therapeutic equipment for Xray. The nominal Xray tube voltages are in the 10 kV to 1 MV range, when connected to alternating mains. It also specifies the specifications for precision and reproducibility of performance in the sense that they relate to radiation quality and the amount of radiation that is produced, and should be taken into consideration as elements of safety. This second edition is a replacement and cancellation of the first edition of IEC 60601-2-8. This edition is a technical revision that brings the standard into conformity with the 3rd edition IEC 60061-1-1 as well as its other specifications. If your firm is involved in the manufacturing of the equipment, we encourage you to visit the site. Check out the most popular cen catalog standards en-iso-28017-2018 info.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
An innovative management system is essential in creating a successful organization today. This is why it is important to pay attention to the regulatory documents that regulate it from the foundation to the end. EN ISO 56002 : 2021 is a prime instance.This document offers guidelines for the establishment, implementation maintenance, and continuous enhancement of an innovative management process for use in all established organizations. This document applies to:A) Organisations who want to achieve sustained growth by proving their capacity and capacity to manage new initiatives effectively in order to produce the outcomes they expect.b. Customers, users, or any other parties that seek to gain confidence in an organization’s innovation capabilities.C. Organizations and interested people who want to enhance communication by establishing a common understanding what constitutes an innovation management system.d. providers that provide training in, assessment, or consulting for, innovation management.e. policymakers seeking to improve the effectiveness and efficiency of support programs aimed at improving the capability of innovation and competitiveness of organizations and advancement of society.1.2 All guidance contained in this document may be used to help anyone.A) All types and sizes of organizations. With the understanding that both established and new organizations can benefit from these rules the focus is placed on the latter.b) any type of innovation, e.g. Any type of innovation which include service, product and process.c) All sorts of strategies, e.g. open and internal innovation market-based, usertechnology and design-driven innovations.It does not describe detailed activities within the organization, rather, it offers guidance at a the general level. It does not set out any specific requirements, tools or strategies for innovation.If one or more amendments in this document misleads you, we recommend you seek out a specialist to find out if this international standard is suitable for implementation into the existing structure of your company, or requires certain amendments and improvements, namely for your situation, selecting a different document that is more suitable within a similar industry. Have a look at the best sist catalog standards sist-en-iso-41011-2018 review.

Characterization Bulk Materials - Determination Size-Weighted Fine Particles And Crystalline Silica Content – Part 3: Sedimentation Method EN 17289-3:2020
In the process of production and the use of various materials, a variety of methods are applied. Each technique requires a particular degree of control based on the amount of work involved. EN 17289-3,2020 is one of the documents which specifies the exact application procedure for crystal silica.This document provides the calculation of the size-weighted percentage (SWFF), as well as the fine fraction of the crystalline silicona (SWFFCS) in bulk materials. It employs the liquid sedimentation technique.This document aims to facilitate users to evaluate bulk material by their weighted size of crystalline silica and fine fraction.This document is suitable to identify bulk crystalline silica materials, as long as it has been fully checked and verified to establish the weighted size of the finefraction as well as crystalline silica.The specification of manufacturing methods makes the process of building a control system. If you're interested in expanding your market reach we suggest you purchase international standards for your facility. See the top clc catalog standards en-136002-1992 site.

Safety - Woodworking Machines Part 10 - Building Site Saws (Contractor Is Aware) (Iso 19085-10 :2018, With Updated Version 2019-12). EN ISO 19085-10:2019/A11:2020
There are certain standards that have added features. This is due to the fact that technologies change constantly, however the design of the document doesn't alter for certain standards. EN ISO 19085-10/2020 is one such document.2020-07-20 JF. The CEN Technical Board approved revised Annex ZA through the C132/2020 decision on the 2020-0708 date, as well as the European Amendment to EN ISO 19085-10. European amendment in the process of publication.You can reach the iTech team if have any queries after you have read this document. Check out the most popular iso catalog standards iso-10207-1991 review.

Health Informatics: Device Interoperability – Part 20701 Point-Of Care Medical Device Communication – Medical Exchange Architecture That Is Service-Oriented And Binding Protocol (Iso/Ieee 11073–20701, 2020) EN ISO 11073-20701:2020
The use of communication technologies is in many areas and not only those directly connected to the field, but also in medical industries. Since the technology for the operation of different devices in medicine is complex and entails the overhaul of existing systems, international standards are being created to aid in these processes. one of them is EN ISO 11073-20701: 2020.
This standard defines a service-oriented design for medical devices, and protocols for communication in medical IT systems. Medical IT systems need to be able to safely and securely control PoC medical gadgets. It describes the functional elements and their communication relationships, as well as how they are connected to protocol specifications.This document is specialized and has been narrowly defined. We recommend to learn more about the technical aspects of this document and speak with managers who are experts in international document selection. Have a look at the recommended iso catalog standards iso-19712-1-2008 information.

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