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发表于 2021-8-28 13:36:30 | 显示全部楼层 |阅读模式


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发表于 2021-9-9 07:36:15 | 显示全部楼层

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发表于 2021-9-28 22:40:50 | 显示全部楼层

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发表于 7 天前 | 显示全部楼层

ISO Standardization Is An Important Element To The Development Of Your Company

Medical Electrical Equipment - Part 2-11: Particular Needs For The Safety Of The Fundamental And Vital Functionality Of Gamma-Beam Therapy Equipment En 60601-2-11:2015
Sometimes, medical devices may be used in treatment. However, they may also cause serious side adverse effects. Equipment is needed in these situations to lessen the chance of negative consequences. EN 60601-2-11.2015 provides an example of such a document. This document refers to the essential safety of gamma radiation therapy equipment. Manufacturers must follow this particular norm from the 60601 series when they design and building gamma beam treatment equipment. To avoid dangerous conditions, the standard specifies tolerance limits for interlocks that must be utilized to stop interruption or termination of radiation. The requirements include tests for type and site as well as tests performed by the company that manufactures. We offer our standard for your business if it is linked to Gamma beam treatment equipment by clicking on the link. Check out the recommended cen catalog standards cen-tr-17225-2018 info.

Innovation Management – Basics And Vocabulary (Iso 56000.2020) EN ISO 56000:2021
Explanatory papers are sometimes required in technical standards. These documents, for instance, describe the issue of information security. EN ISO 56000: 2021 is an excellent example. This document outlines the fundamental concepts, vocabulary and the principles of innovation management as well as their methodical implementation. This document can be used to:a) companies that have implemented an innovation management program or conducting assessment of innovation managementB. Organisations that require help in managing innovation activitiesc) Customers, users, and other interested parties (e.g. suppliers, partners, funding organisations and universities, investors and public authorities, etc.) who wish to have confidence in the capabilities of innovation and performance of an organisation.D. organisations and other individuals who wish to improve communication via an understanding of the innovation management terminology;(e) Providers for training in assessment, or for consulting regarding innovation management and its methods.F. Developers and users of similar standards for innovation management.1.2 This document will be applicable to:b) any type of innovation, e.g. Product, service, model, and method can be considered in any order, from the incremental to the radical.c. All methods, e.g. c) all types of approaches, e.g., internal and external innovations, market-based technological and design-driven developments.This document specifies the definitions and terms that apply to all innovation management and management system requirements developed by ISO/TC 279.This standard provides a number of important clarifications. We recommend that your read them carefully and cross-check the standards with your knowledge base to be sure they're the right document to utilize to promote your business on a global scale. Check out the best cen catalog standards pren-14015 info.

Analyzing And Determining Bulk Materials And Crystalline Silica Content. Part 1. General Information And Choices Of Test Procedures EN 17289-1:2020
The wide range of materials used in production creates a challenge for regulation locally as well as globally. International standards are currently being created to ease the entry of businesses and organizations into new markets.This document provides the specifications and choices of testing methods for the determination of the fine fraction of crystalline silica (SWFFCS), and the size-weighted small fraction (SWFF).This document includes guidance on the preparation and determination using Fourier Transform Infrared Spectroscopy and X-ray Pulsed Diffractometry.EN 1789-2 explains how to calculate the size-weighted portion of fine particles from a measured size distribution. It assumes the particle size distribution of the crystalline quartz particles is identical to those of other particles in the bulk material. EN 1789-3 describes the liquid sedimentation process to determine the size weighted fine silica fraction of crystal. Both methods have limitations and assumptions which are described in EN 17289-2 as well as EN 1789-3. If validated and investigated using the EN 17289-3 method may be utilized to calculate additional constituents.This document can be used to describe crystalline silicona containing bulk materials that have been thoroughly studied and validated in order to assess the size-weighted, fine fraction, as well as crystallinesilica.Your company's technological documentation base is greatly enhanced by your activities that come into contact with the information contained in this article. More information is available on our website. Check out the top sist catalog standards sist-en-17186-2019 info.

Machine Tools Safety - Safety For Presses Part 4 : The Safety Requirements Of Pneumatic Presses. (Iso 16092-4.2019). EN ISO 16092-4:2020
Safety issues are an essential part of creating the regulatory framework needed for any production or organization. This is the reason why there is a lot of international standards which address this topic.This document, as well as ISO 16092-1, defines the safety standards for technical people who are involved in the development, production and distribution of pneumatic presses that are specifically designed to work with cold metal, or partially from cold metal.This document addresses the various risks that could affect pneumatic presses when they are used in accordance to their intended purpose and in conditions that are reasonably predicted by the maker (see Clause 4.) All phases, in accordance with ISO 12100:2010, 5.4 are considered.If you're interested in buying this document, click the link below to view all the technical specifications. Reach out to the team that will provide all the details. Have a look at the most popular cen catalog standards en-13210-2004 info.

Health Informatics -- Requirements For International Machine-Readable Coding Of Medicinal Product Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies develop and improved, there will be more rules to regulate their use and reduce risks. One example of such documents that is able of changing due to the rapid development of new technologies, is EN ISO 11073/10201 / IEEE 11073: 2020.This document provides guidelines on the identification and labeling of medicinal products starting from the point of manufacturing of the medicinal product packaged to the point at which you can dispensing the product. This document offers best practices to use AIDC barcoding systems. The coding interoperability specifications for different AIDC technologies are also looked at by users, e.g. Radio Frequency Identification (RFID).If you've used this guideline and are operating in the same field we suggest you purchase the latest version that has updated guidelines. Have a look at the recommended etsi catalog standards etsi-ts-103-221-1-v1.5.1-2019-07 blog.

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