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发表于 2021-6-8 09:02:01 | 显示全部楼层 |阅读模式
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发表于 2021-9-29 02:30:11 | 显示全部楼层

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发表于 2021-10-13 23:52:02 | 显示全部楼层

ISO Standardization Is An Essential Step In Your Business's Development

Part 1-9 Of Medical Electrical Equipment - General Requirements For Safety And Fundamental Performance – Collateral Standard  Requirements For Eco-Friendly Design En 60601-1-9:2008
The environment is all about the health of all living creatures on Earth. Although technology is constantly improving, the primary goal should be to ensure that new systems remain secure. That's why there are new standards for medical equipment, which regulate the environmental impact. This collateral standard has the goal of improving the environmental impact of all medical electrical devices. It considers specifications for the product, its manufacturing, design logistics, installation use; end-of-life management. This means protecting the environment and human health from hazardous substances, conserving raw materials and energy and minimizing the production of waste, as well as minimizing adverse environmental impacts associated with the disposal of waste. These requirements must be included in all phases of the lifecycle of medical electronic equipment, beginning from the design stage to the final management. Follow the link to the website for more detailed details about this crucial document. Check out the top cen catalog standards en-isp-10608-6-1996 site.

Innovation Management - Fundamentals And Vocabulary (Iso 56000 :2020). EN ISO 56000:2021
Sometimes, documentation is created in order to avoid confusion about technical standards, like, for instance concerns with security of information. EN ISO 56000: 2021 is a notable example. This document outlines the fundamental concepts, terms and fundamentals of innovation management, as well as their methodical implementation. It can be used to:A) Companies which have implemented an innovation management system;b) organisations that require to increase their capability to efficiently manage innovation;C. Customers customers, users, and other relevant parties (e.g. Partners, suppliers, funders university, investors, public authorities, etc.) who want to have confidence in the innovation capabilities and efficiency of an organization.d. organizations and other those who wish to enhance communication by establishing a common understanding for the terms employed in innovation administrationE) Training providers for assessments, training, or consultation regarding innovation management and its processes.F. Developers of innovation management standards and other related standards1.2 This document can be used to be used to. Any type of organization regardless of their nature and maturity level, sector or size.b. Innovations of all kinds, e.g. Service, product, model and method could all be considered from the incremental to the radical.c. All methods (e.g. open and internal innovation, user-, market-, technology- and design-driven innovation.This document provides the definitions employed in all ISO/TC279 standards related to innovation management.There are numerous clarifying aspects in this document. We recommend that you study them carefully and evaluate them against the technology foundations of your business in order to ensure that the document will be able to help you promote your business to the highest possible level. Have a look at the best cen catalog standards cen-iso-ts-19321-2020 info.

Characterization Of Bulk Materials - Determination Of The Size-Weighted Fine Fraction As Well As The Content Of Crystalline Silica - Part 1 General Information And Selection Of Testing Methods EN 17289-1:2020
The variety of products and materials complicates regulation both locally, and globally. International standards have been developed to ease companies and organisations entering new markets. One of these is EN 17289-1:2020.This document outlines the requirements and testing options to determine the fine portion of crystalline silicona (SWFFCS) and the size-weighted small fraction (SWFF).This document gives also guidance on the preparation of the sample and determination of crystallized silica through X-ray Powder Diffractometry (XRD) as well as Fourier Transform Infrared Spectroscopy (FT-IR).EN 1789-2 explains how to calculate the size-weighted fraction of fine particles based on the size distribution that is measured. It is based on the assumption that the size distribution for the crystalline quartz particles is exactly the same as that of other particles found in the bulk material. EN 1789-3 describes a procedure using a liquid sedimentation technique to calculate the size-weighted percentage of crystalline silica. Both methods are restricted in their scope and rely on certain assumptions. The method in EN 17289-3 may be utilized for different constituents other than CS in the event that it is researched and verified.This document is applicable to bulk substances that have been thoroughly studied and verified for the determination of the fine fraction that is weighted by size or crystal silica.The presence of the technology documentation base will assist you scale up production if your area of activity is in direct contact with the materials described in the document. For more information, you can follow the link to our website. Have a look at the most popular clc catalog standards en-60309-1-1999-a1-2007 information.

Mechanical Products - Methodology To Less Environmental Impact During The Process Of Designing And Developing Products EN 16524:2020
As new technologies and air pollution become more prevalent also, so are environmental and safety concerns. EN 16524:2020 is one of the documents that provides an answer.This document outlines a method to reduce the environmental footprint of product design and production. This is applicable only to mechanical products, as detailed in 3.1.This method is particularly useful to redesign existing products. It could be employed to develop new products if you have the correct assumptions about the (virtual reference) product. It is applicable to companies that integrate ecodesign to reduce environmental impacts throughout the product life cycle. This also includes other factors like product performance, quality, price, etc.It fulfills some of the requirements in ISO 14001 :2015 regarding the incorporation of environmental aspects into product design. This document is targeted at people who are directly involved in the development and design of mechanical products and managers responsible for defining corporate policies and decisions. The method proposed is designed as part to incite the companies to engage in ecodesign.This document includes an example for companies to make use of in their marketing about the environmental approach. This document is not designed to be used to evaluate the products of different suppliers. The document isn't intended to be used for certification of products.This document is important, especially in the 21st century. You should therefore be aware of the possibility of buying it and introducing it into your business. See the top rated iec catalog standards iec-61671-5-2016 info.

Health InformaticsInteroperability Between Devices. Part 20701-Point-Of-Care Medical Communication. Service Oriented Medical Devices Exchange Architecture And Protocol Binding. (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
Communications technologies are utilized not just in the areas that are most closely related to this area as well as in the medical industry. The introduction of different medical devices demands a complex transformation. To ease these processes international documents have been made.
This standard is an architecture for medical devices that is service-oriented and communication Protocol Specification for distributed Systems of Point-of-Care(PoC) and medical devices and medical IT Systems that need to exchange data and regulate PoC networked medical devices. It specifies the functional elements, their communication relations, as well the connecting of these components and their communication relations to protocol specifications.The document is specific and limited in the scope. This is why we suggest that the document be reviewed for more information. If you have questions, you can consult with managers who are experts in international document selection. Check out the most popular sist catalog standards sist-en-2997-011-2020 blog.

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