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发表于 2021-8-18 22:59:04 | 显示全部楼层 |阅读模式
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发表于 2021-9-29 01:40:41 | 显示全部楼层

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发表于 2021-10-4 23:02:52 | 显示全部楼层

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发表于 2021-10-14 00:14:22 | 显示全部楼层

ISO Standardization Is Essential For Business Growth

Part 1-9 Of Medical Electrical Equipment - General Safety Requirements And The Essential Performance – Collateral Standard : Requirements In Environmental-Friendly Design En 60601-1-9:2008
Environment means the protection of all living beings. As technology continues to evolve one of the most important things to be doing is to make sure that the new technology is secure. The new standards for the safety of medical equipment in terms of environmental protection have been developed to tackle this issue. This collateral standard was created to improve environmental safety for medical electrical equipment. This means protecting the environment and the people's health from harmful substances, while conserving raw materials and energy, minimising the production of waste, and minimizing the negative environmental impacts caused by it. From the time of specification to the end of equipment management, the criteria needed to reach this goal must be considered. Visit the website to learn more details about this crucial document. Check out the best etsi catalog standards etsi-en-303-645-v2.1.1-2020-06 information.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
An innovative management system is crucial to developing a profitable organization today. This is why it is so important to pay attention to the legal documents that govern it from the beginning to the last stage. EN ISO 56002: 2021 is a prime example.This document provides guidance on how to establish and maintain, establish and enhance the effectiveness of an innovation management program that is applicable in all organizations. It can be used for:A) Companies that wish to have sustained success by proving their ability and capacity to manage new actions effectively to achieve the expected outcomes.B. Customers and users who are curious about the company's innovative capabilities.C. Organizations and interested parties looking to improve communication through a shared understanding of what makes an innovation management system.D) Consultants as well as training, assessment and advice on innovation management and systems.E) the policy makers, with a view for higher effectiveness of assistance programs that focus on the capabilities of innovation and competitiveness of companies and growth of society.1.2 All the guidance within this document is general and is intended to be relevant to:All kinds of businesses regardless of size, sector, or type. While our primary focus is on established companies however, we acknowledge that temporary and permanent businesses could benefit from these rules in part or in their entirety.b) All types of innovation, e.g. The service, product or process can be described as a model, process, product, or method. These innovations may be categorized as incremental or radical.C) All types of approaches, e.g. Internal and open innovation, user-market-, technologyand design-driven innovations.It doesn't describe the activities within an organization It provides guidelines at a general scale. It does not prescribe specific tools or methods to encourage innovation.If you're confused by some of the modifications in this document, we suggest you speak with an expert to verify whether the international standard is suitable to be implemented within your company's current structure. See the top iec catalog standards iso-80601-2-67-2020 site.

Characterization Of Bulk Materials - Determination A Size-Weighted Fine Fraction, Crystalline Silica And Crystalline Silicon Content - Part I General Information And The Choice Of Tests EN 17289-1:2020
Regulators are complex locally as well as globally due to the vast range of materials used in production. To facilitate the entry of businesses and organizations to new markets, international standards are being developed among them EN 17289-1:2020.This document specifies the criteria and the test method for the determination of the size-weighted fine portion (SWFF) and the size-weighted fine fraction of silica crystalline (SWFFCS) in bulk materials.This document also provides guidance on the preparation of the sample and for the identification of crystallized silicona with Xray Diffractometry XRD (XRD) and Fourier Transform Infrared Spectroscopy FT-IR (FT-IR).EN 17289-2 outlines a method to calculate the size-weighted fine percent using a measured particle size distribution. However, it assumes that the sizes of the crystalline particles are identical to those found in bulk material. EN 17289-3 describes how to calculate the size-weighted fine percentage of crystalline silicona using liquid sedimentation. Both methods are based upon a number of limitations and assumptions, which are listed in EN 17289-2 and EN 1789-3 and EN 17289-3, respectively. The EN 17289-3 method could be suitable for other constituents that are not CS when confirmed.This document covers crystallized silica with bulk material that has been thoroughly investigated and validated for the assessment of the size-weighted, fine fraction as well as the crystallized silica.If your business comes into contact with the materials mentioned in the description of this document, then its presence in the documentation base for technology of your business will significantly facilitate the process of scaling up production. Visit our website to learn more. See the recommended cen catalog standards en-809-1998a1-2009-ac-2010 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 concerns are always at the forefront of any regulatory framework.This document is in addition to ISO 16092-1. It specifies the technical safety measures and the requirements to be followed by anyone involved in designing, manufacturing, and supplying pneumatic presses intended to operate with cold or partly cold metal.This document details all hazards that could impact pneumatic presses in the event that they are not used in the manner intended or in circumstances of misuse that are reasonably predicted by the maker (see the clause 4). Each phase of the life of the machine as described in ISO 12100:2010, 5.4, have been taken into account.If you're interested in purchasing the document, simply follow the link to obtain all the technical information. You can also contact the team to clarify any doubts. Have a look at the best cen catalog standards en-iso-23874-2018 information.

Health Informatics -- Requirements For International Machine-Readable Codes For Medical Package Identifiers For Products ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies develop on the planet and more rules governing their use and minimising risks are created. One example of such documents, which is amenable to revision due to new developments such as EN ISO 11073/10201 / IEEE 11073: 2020.This document outlines guidelines for identifying and labelling medical products from the moment where they are intended to be dispensable. This document offers best practices to use AIDC barcoding systems. However, users should take into consideration the requirements for interoperability in coding for different AIDC technologies, e.g. Radio Frequency IdentificationIf you've previously employed a previous version of this document, and are continuing to operate in the same field of operation we strongly recommend buying this document with updated recommendations and international guidelines. Have a look at the recommended cen catalog standards en-iso-19403-6-2020 blog.

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发表于 2021-10-14 01:05:26 | 显示全部楼层

ISO Standardization Is A Key To The Growth Of Your Company

Part 1: Safety Specifications And Performance Requirements For Medical Electrical Equipment. Collateral Standard - Electromagnetic Disturbances. Tests And Requirements En 60601-1-2:2015
Specification of medical equipment requires greater specificity and detail. Every medical system is subject to its own specifications. This document covers the safety basics and performance of Medical Equipment (ME) equipment and ME systems in the event of electromagnetic disturbances and to electromagnetic disturbances emitted from medical equipment and systems. The first elements of this standard to be useful in understanding the safety requirements for medical equipment use. See the recommended iec catalog standards iec-61557-13-2011 information.

Innovation Management Tools And Techniques For Innovation Partnership Guidelines (Iso 56003:2019) En Iso 56003:2021
A key role in the creation of new products is to establish the ideal collaboration. Through this type of partnership, it's possible for individuals to share their ideas, ideas, and resources, assistance, and other aspects that are crucial to developing a new system. EN ISO56003 2021 is an international standard that sets out guidelines for the creation of partnerships that are productive.This document provides a guidance for partnerships in the field of innovation. It gives instructions on how to establish partnership in the field of innovation.Deciding whether to enter an Innovation PartnershipFind, evaluate, and select your partners• ensure that the perceptions of value are aligned and challenges for the partnership,Control the interactions with your partnersThe guidelines provided in this document can be used for any kind of partnership and collaborations . It is designed to be applicable to all organizations regardless of their type, size, product/service offered, for example:A) startups that collaborate with larger corporations;b. SME or larger companiesc. private sector companies that are academic, public entitiesd) public, academic, or non-profit institutions.The first step in forming a partnership for innovation is to analyze the gaps. Then, you must discover and connect potential partners. And lastly, manage their interactions.This is a great standard for both startups as well as established businesses. Since partnership is essential for the success of scaling and development this is an issue that applies to all cases. If your business is looking for growth over the long run this document is crucial. See the most popular iso catalog standards iso-dis-10667-2 information.

Characterization Of Bulk Materials - Determination Of A Size Weighted Fine Fraction, Crystalline Silica And Crystalline Silica Contents Part 3 - Sedimentation Method EN 17289-3:2020
Numerous methods are employed for the manufacture of different materials and their application. Each method requires a specific level of regulation depending upon the extent of the activity. EN 17289-3 is 2020. It specifies the method for applying the crystalline silica.This document will help you determine the sizes-weighted fine fraction (SWFF) of crystalline Silica in bulk materials.This document was designed for users to help them evaluate bulk materials according to their finefractions weighted according to size, as well as their silicon content.This document applies to crystalline silica containing bulk substances that have been fully evaluated and verified for evaluation and weighted size of the fine fraction.The specification of manufacturing methods makes the process for building a control system. We strongly recommend purchasing international standards when you are trying to expand into new markets. Have a look at the recommended cen catalog standards en-14262-2003 information.

Methodology To Reduce The Environmental Impact Of The Development Of Products And In The Design Of Mechanical Products EN 16524:2020
Safety and environmental issues are growing with the advent of new technology and air pollution emerge. EN 1654: 2020 is a document that could assist in solving this issue.This document provides a strategy to reduce the environmental footprint of product design and production. This is applicable to only mechanical products as described in 3.1.This method is ideal for revising an existing product. If assumptions about the virtual product are made, the method can be applied to design an entirely new product. This is a method for companies who have decided to adopt an ecodesign approach to maximize environmental impact throughout the product's life cycle. Additionally, it addresses other aspects of the product, like functionality, cost, and quality.It assists in meeting the specifications of ISO 14001, 2015 on the incorporation of environmental aspects into the design of products. 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 decision-makers. The approach is intended to encourage ecodesign efforts within companies.This document provides the template that companies can utilize in their communications about the environmental approach. This document is not designed to be used to compare products of different suppliers. This document is not appropriate for product certification.This document is relevant especially in the 21st century. That is the reason you must be aware of the possibility of having it , and then integrating it into the operations of your business. Have a look at the recommended cen catalog standards en-1004-2004 info.

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
Documents regarding maintenance and use of devices in medicine, like any other standard has many parts. These parts can be used in conjunction with one another or talk about entirely different technologies. EN ISO 11073-10201 / IEEE 11073-10201 2020.The scope of this project is to define a general object-oriented information model that can be used to arrange information and identify services used in the point-of-care (POC) medical device communications. The project's focus is focused upon acute care medical devices as well as the information for communication that is derived from vital patient signs.Information technology is increasingly used to expand business and increase productivity. We recommend that you look into purchasing documents that will standardize their use globally. Have a look at the recommended sist catalog standards sist-en-15327-1-2008 review.

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