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发表于 2021-10-10 08:08:08 | 显示全部楼层
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发表于 2021-10-14 00:38:50 | 显示全部楼层

ISO Standardization Is Crucial To The Development Of Your Company

Part 2-8 Of Medical Electrical Equipment: Specific Specifications For The Safety And Vital Performance Of Therapeutic Xray Equipment Operating Within The 10 Kv- 1 Range Of Mv. En 60601-2-8:2015
Many reasons can explain why businesses are prone to disregard specific rules or even documents. One reason is the fact that standards are constantly changing. One of very important documents that could affect the industry that deals with medical equipment is EN 60601-2-8:2015. It lays down specific safety and essential performance requirements for therapeutic X-ray equipment that has nominal X-ray tube voltages within the range 10 kV to 1 MV when connected to alternating current supply mains. It outlines the requirements for reliability and accuracy which are directly connected to the quality of radiation. The second edition of IEC 60601-2-8 has been rescinded and replaced with this edition. This revision in technical terms makes the standard more in line with IEC 60601-1's 3rd edition and all of its other collateral standards. We strongly recommend to follow the hyperlink to the site if your company acts in the field of the mentioned equipment. Have a look at the most popular iso catalog standards iso-1751-1993 blog.

Innovation Management - Fundamentals And Vocabulary. (Iso 56000.2020). EN ISO 56000:2021
Explanatory documentation are sometimes created in order to avoid misconceptions about technical standards such as, for instance, the issue regarding information security. EN ISO 56000: 2021 is one such example. This document provides the basic, concepts, and principles to manage innovation and its systematic execution. It can be used for:A) Companies who have implemented an innovative management system;B. Companies that require assistance in managing innovation activitiesC. Users, customers, and other relevant parties (e.g. suppliers, partners, funding organisations, investors, universities or public authorities, etc.) who want to have faith in the ability to innovate and the performance of the company.d. organizations and other those who wish to enhance communication by establishing an agreed-upon understanding of the terms that is used in innovation administratione) Consulting and training, assessment, and advice on innovation management and systems.F. Innovation management standards and related standards1.2 This document will apply to:b. All types, including disruptive innovation. All types of innovations, including product, service and model. They may be incremental or radical.C. All types of approaches including. open and internal innovation, market-based, usertechnology-, and design-driven innovations.This document defines the terms and definitions that are applicable to all ISO/TC 279.-developed standards for management of innovation and management systems.This standard contains many crucial clarifications. We suggest that you read them carefully and cross-check their accuracy with your technological base in order to be sure that they are the right document to use to promote your organisation on a global scale. Have a look at the top rated iec catalog standards iec-60705-2010-amd2-2018 blog.

The Characterisation Of Bulk Materials - Determination Of An Amount-Weighted Fine Fraction, And Crystalline Silica Content - Part 2: Calculation Method EN 17289-2:2020
Different parts of the same standard may complement each other and regulate completely different areas of application of the same substance. EN 17178-2 2020 is the second part of the standard that was previously in use.This document explains how bulk materials can be used to calculate the size-weighted portion of fine silica (SWFFF) as well as the fine fraction of size-weighted crystal silica (SWFFCS). The document also outlines the preconditions and assumptions to be met in order for this method be valid.This document offers details that can assist users in assessing bulk materials in relation to their size-weighted crystalline size and fine fraction.Annexe A contains a particular method to determine the SWFF of diatomaceous earth bulk materials. Annex A offers an illustration of how to assess the SWFF for diatomaceous rocks bulk materials.This document is suitable for crystalline silica containing bulk materials that have been fully studied and verified for the assessment of the size-weighted fraction and crystalline silica.It is possible to get a better idea of the importance of these standards through comparing the technical parameters of production standard with those of individual standards. If you have any questions regarding the process of implementing this stage you can always seek out a team comprised of specialists in the field that use international standards. Have a look at the top cen catalog standards en-1116-2018 site.

Safety - Woodworking Machines - Part 10 - Saws For Building Sites (Contractor Is Aware) (Iso 19085-10 :2018, With A Corrected Version For 2019-12). EN ISO 19085-10:2019/A11:2020
Certain standards have additions that are created because technologies are evolving and in the same way, the initial appearance of an already in place standard remains the same. One such document is EN ISO 1905-10: 2019 / A11: 2020.2020-07-20 CF: 2020-07-20 C 2020-07-20 CP the C132/2020 adopted on 202007-08, CEN Technical Board endorsed the updated Annex ZA. This was in line with the European Amendment, EN ISO 1908-10: 2019. European Amendments are being released.If you have questions in reading this article, feel free to email the iTech department to help you answer your questions. See the top rated cen catalog standards en-iso-8130-1-2019 review.

Information Technology For Health -- International Machine-Readable Coding Requirements For Medicinal Product Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies are developed and improved, there will be more rules to regulate their use and reduce risks. EN ISO / IEEE 11073-10201 2020 is an example of such documents. It is easily upgradable in response to the latest developments.This document contains guidelines for identifying and labelling of medicinal products, starting at the point of making the packaged medicine until the time where it is dispensing. This document provides best practices for AIDC barcoding technologies. The specifications for coding interoperability for different AIDC technologies could be taken into consideration by the users, e.g. Radio Frequency IdentificationIf you've previously utilized a prior version of this document and continue to be within the same area of work, we strongly recommend purchasing this document with updated recommendations and international rules. Check out the recommended cen catalog standards en-13257-2014a1-2015 site.

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