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发表于 2021-10-13 22:39:19 |显示全部楼层

ISO Standardization Is A Key To The Growth Of Your Business

Part 2-6 Part 2-6 - Medical Electrical Equipment: Special Requirements For The Safety And Performance Of Microwave Therapy Equipment En 60601-2-6:2015
EN 60601-2-6 2015 is yet another significant document that regulates equipment production and usage. It specifies the minimum requirements needed to ensure that microwave therapy equipment is safe to use. This particular standard modifies and enhances IEC6061-1 (third edition 2005, amendment 1st of 2012). This second edition replaces 1984 first edition IEC 60601-2-6. This is a reminder that keeping up-to-date with new standards could affect the perception of your company as well as the efficiency of your business in the marketplace. Have a look at the most popular cen catalog standards pren-12184 review.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Innovative management systems are vital to build a successful business structure. That is why it's crucial to pay close attention to the regulatory documents that regulate it, from its beginning to its final stage. EN ISO 56002: 2021 is just one of them.This document provides guidance regarding the development, maintenance and continuous development of an effective management method that can be utilized by all organisations. It is applicable to:Companies that can demonstrate their capability to effectively manage their innovation processes in order to reach their goals.b. Customers and users who are curious about the organization's innovation capabilities.c. Organisations and other interested individuals looking to improve communication through a shared understanding of what makes an innovation management system.D) Consultants and training, assessment, and consultation for innovation management and systems.e) policy makers, aiming for higher effectiveness of support programs targeting the capabilities of innovation and competitiveness of companies and advancement of society.1.2 The guidance in this document may be used to guide anyone.It is a) any type of organization regardless of their type, sector, or size. While the main focus is on established companies but we also recognize that permanent and temporary organizations can benefit from these guidelines in some or all of their entire.b. All kinds, including disruptive technological innovations. You may choose to make innovative or radical ideas for product, service.c) All kinds of approaches, e.g. c) All kinds of strategies, e.g., internal and external innovation, market- and technology-based innovation and design-driven innovation.It does not describe detailed processes within the company, but rather provides guidance at the general level. It doesn't include any requirements, tools or methods that can be utilized to create new activities.If you believe that some sections of this document seem to be misleading it's a good idea to consult an expert. They will help you decide if the international standard is suitable for implementation in your existing structure. Check out the best sist catalog standards sist-en-10025-4-2019 site.

The Calculation And Characterisation Of Bulk Materials EN 17289-2:2020
Each part of a standard may be used together with other parts and can regulate completely different areas of use of the material. EN 17178-2 2020 is the second part of the earlier standard.This document describes how to determine bulk materials' size-weighted-fine percentage (SWFFF) as well as its size-weighted fine percentage of crystalline silica (SWFFCS). This document also outlines the prerequisites and assumptions that must be fulfilled for this method to be valid.This document was created to assist users in evaluating bulk materials based on their finefraction size weighted by size as well as their silicon content.Annexe A provides a precise method for evaluating SWFFs for bulk materials diatomaceous. The Annex A has specific instructions for evaluating the SWFF of diatomaceous earth bulk materials. This is because of the porosity inside.This document is applicable to crystallized silicona that contains bulk materials that have been thoroughly studied and validated in order to assess the size-weighted, fine fraction as well as crystalsilica.To better understand the necessity of these standards, it is vital to examine the technical parameters utilized in production standards with the specifications of individual standards. For any questions concerning the implementation of this stage you can always consult a team made up of professionals in the field that use international standards. See the most popular iec catalog standards iec-61754-35-2020 site.

Software Engineering Systems - Software Product Quality Requirements Evaluations (Square). Common Industry Formats (Cif) For Usability. User Requirements Specifications (Iso 25065.2019). EN ISO 25065:2020
The quality of software is now the primary factor for ensuring a position of leadership on international markets. To comprehend the rules of these markets it is important to review the international requirements. These requirements are contained in documents like EN ISO 25065 2020.This document provides a framework and consistent terminology for describing the requirements of users. It defines the standard industry format (CIF) that is used to define the requirements of users. This is inclusive of the content elements as well as the manner of expressing those specifications.A specification of the user's specifications is the formal documentation the requirements of a user. This aids in the design and evaluation of interactive systems.User requirements are defined as the following: a) the requirements of user interaction with the system in order to get the desired results (including the requirements for outputs of the system, attributes and their attributes) and; b) the use-related quality specifications which define the quality standards for the outcomes of users interfacing with the interactive systems . They can also be used for system acceptance.ISO/IEC 25030 defines quality requirements. This document includes a special type of quality obligation, namely the usage-related requirements. The elements that constitute the User Requirements Specification can be used as part of documentation that result from ISO 9241-210 activities or design methodologies that are human-centered like ISO 9241-220.This document is designed for use by requirements engineers and business analysts, product mangers and product owners and others who acquires systems from third party. CIF's standards cover information related to usability (as specified in ISO 9241-11 and ISO/IEC TR25060).User requirements might not just be about usability, but they could also include other perspectives like human-centred quality, ISO 9241-220, ISO/IEC 25011, ISO/IEC 25030, and other quality perspectives within ISO/IEC 25010.While this document was created for interactive systems, it could be used in other areas. The document does not prescribe any kind of process, lifecycle, or methodology. The components of the User Requirements Specification could be used in iterative Development, which is the elaboration of and the evolution (e.g. as in agile development).
This international standard will make your professional activity considerably more simple. It can also assist to structure the existing system, and open up new opportunities for expanding your business's reach and market expansion. See the most popular cen catalog standards en-13166-2012a2-2016 site.

Health Informatics, Device Interoperability. Part. 200701; Point Of-Care Medical Device Communication. Architecture For Exchange Of Medical Instruments That Is Service-Oriented. Protocol Binding (Iso/Ieee 11073–20701 2020). EN ISO 11073-20701:2020
Communications technologies are utilized in many areas, not just those that are directly related to this industry as well as in medical fields. Because the operation of various devices in medicine is complex and involves the overhaul of existing systems, international standards are being created to aid in these processes. one of them is EN ISO 11073-20701: 2020.
This standard is a service-oriented Medical Device Architecture and Communication Protocol Specification for distributed System of Point-of-Care(PoC) and medical devices, and medical IT Systems that need to exchange data and control PoC connected medical devices. It defines the functional elements as well as the communication relations and the binding to protocol specifications.This document is a bit narrow-profile and specialized, which is why we recommend that you become familiar with its technical specifications in more depth and If you have any questions, consult with managers who specialize in the choice of international documents. Check out the most popular iso catalog tc iso-tc-21-sc-3-wg-11 information.

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