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发表于 2021-10-4 23:35:58 | 显示全部楼层 |阅读模式
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ISO Standardization Is A Key To The Growth Of Your Company

Part 1-10 Of Medical Electrical Equipment: Essential Safety And Performance - Collateral Standard. The Requirements For Designing Closed-Loop Physiologic Controllers En 60601-1-10:2008
Production of different elements is essential to ensure the general safety of using medical equipment that is applied. Not only are standards created for the use of medical equipment however, they also govern its manufacture. This implies that knowledge of new standards for medical equipment is at the same level of importance as the general ones. EN 60601-1-10.2008 specifies the requirements for the creation of a control system that controls an physiologic parameter. It also applies to other kinds of PCLC (e.g. The collateral standard is applicable to all types of closed-loop controllers, such as fuzzy, adaptive, and linear. In case you are interested in this document, contact Iteh. Check out the top rated cen catalog standards en-12312-2-2014 blog.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Innovative management systems are essential for establishing a profitable business structure. That is why it's so important to keep a close eye on the legal documents that govern it, from the beginning to the final phase. One of them is the internationally recognized standard EN ISO 56002: 2021.This document provides instructions to help you design an, establish, maintain and constantly enhance your innovation management process. It is a useful tool to be utilized by all existing organizations. This document is applicable to:a) organizations seeking sustained success by developing and demonstrating their ability to effectively handle innovation initiatives to reach the desired outcomesb. Customers, users or any other parties looking to be confident in the organization's ability to innovate.C. Interesing parties and organizations who seek to improve communication with one another by sharing common understanding of what is an innovation management plan.D) Providers of consulting and training, assessment, and consulting for Innovation management systems and processes.e. Policy makers, who seek to improve their effectiveness in implementing programs that target innovation capabilities and competitiveness organizations as well as the development society.1.2 The information contained in this document is general and is designed to be applicable to:A. All kinds of organizations regardless of size, sector, type or. While the guidelines are intended primarily for established organizations but they can be applied in any and all instances for start-ups as well as temporary companies.b) any type of innovation, e.g. product, service, process, model, and method that range from small to radical;c) All sorts of strategies, e.g. open and internal innovation, market-based, usertechnology, and design-driven innovations.It doesn't describe the specifics of an organization's activities, but it provides guidance on a general scale. It does NOT recommend specific tools or strategies for innovation.If you're confused by some of the modifications in this document, we recommend that you talk to a specialist to confirm whether the international standard is appropriate to be implemented in your organization's current structure. See the most popular etsi catalog standards etsi-sr-003-292-v1-2-1-2018-09 blog.

The Characterisation Of Bulk Materials – Determination Of A Size Weighted Fine Fraction Or Crystalline Silica Contents - Part 2 Method For Calculation EN 17289-2:2020
A number of parts can be combined to create a single standard that covers completely different areas. EN 17289-2: 2020 is the second part of the standard that was previously in use.This document describes how to calculate the size-weighted crystalline silica fine fraction (SWFFF) and the fine fraction that is weighted by size (SWFFCS) for bulk materials. This document also outlines the necessary assumptions and requirements for this method.This document offers information that will help users assess bulk materials in terms their size-weighted crystalline and fine fraction.A specific method of assessment of the SWFF for bulk diatomaceous earth materials can be found in Annex A. Due to the porosity inside diatomaceous earth, the general guidelines given in this document are adapted in order to consider the material's effective density.This document can be used for bulk silica-containing crystalline materials which have been fully investigated and validated for the analysis of the size-weighted fraction and the crystalline silica.To get a better understanding of the necessity to implement the standards, it's essential to examine the technical parameters of production standards with the requirements of the individual standards. If you have any concerns regarding the implementation of this stage you can always seek out a team comprised of professionals from the industry which uses international standards. Have a look at the top iso catalog standards iso-4282-1977 information.

Methodology To Minimize The Environmental Impact Of Product Design And Production Of Mechanical Products EN 16524:2020
As new technology is developed and air pollution becomes more reported Environmental and safety concerns are always evolving. EN 16524:2020 is one document that proposes a solution.This document outlines how to lessen the impact on the environment of product design and development. It is designed to mechanical products in accordance with 3.1.This methodology is particularly well suited to the redesign of an existing product, but it can also be applied for the design of a new product provided the appropriate assumptions about the (virtual) model are taken. This methodology is intended to be used by companies that are adopting an ecodesign method to minimize the impact on the environment during the lifecycle of their products.It also meets the requirements of ISO 14001 2015 regarding the incorporation of environmental considerations into the design of products. This document is aimed at people directly involved in the creation and development mechanical products. It is also aimed at managers and decision-makers accountable for corporate policies and decisions. The intention is to stimulate ecodesign initiatives in companies, as part in a teaching-based continuous improvement approach.This document also contains templates that businesses can utilize for communicating their environment approach. This document is not intended to be used for comparison of products (even similar) from different suppliers. This document is not intended or suitable for certification purposes.This document is especially relevant in the 21st-century, so you should consider the possibility of purchasing the document and integrate it into the business activities of your organization. Check out the top etsi catalog standards etsi-ts-136-579-2-v14-9-1-2021-01 blog.

Health Informatics Interoperability Of Devices. Part 101: Point Of Care Medical Device Communication. Domain Information Model. Iso/Ieee 11073-10201:2020. EN ISO/IEEE 11073-10201:2020
Like any other standard, documents pertaining to the usage of devices in medical practice have different parts that can both be a complement and also talk about completely different technologies. One example is EN ISO /IEEE 11073-10201: 2020.The goal of this project is to create a general data model, based on object-oriented concepts, that could be used to identify and organize medical device communication at the point of care (POC). The project is focused mainly on medical devices for acute care as well as the communication of vital signs and information.As information technology becomes more used in expanding businesses and increasing productivity, we recommend that you think about purchasing documents that can be used to standardize their usage internationally. See the most popular cen catalog standards en-13725-2003 review.

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