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قديم 09-23-2021, 08:00 PM   رقم المشاركة : [12]
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Part 2-6 - Medical Electrical Equipment: Special Rules For The Security And Essential Performance Microwave Therapy Equipment En 60601-2-6:2015
EN 60601-2-6 :2015 is another document that regulates medical equipment manufacturing and usage. It describes the essential requirements for the safe operation of microwave treatment equipment. This particular standard is a supplement to and modifies IEC 60601-1 (third edition., 2005; amendment 1, 2012). This second edition replaces 1984 first edition IEC 60601-2-6. It is yet another reminder that it is important to stay up-to-date with the latest standards for your business' image as well as the productivity of your market performance. Have a look at the top iso catalog standards iso-9505-1992 review.

Innovation Management - Fundamentals & Vocabulary (Iso 56000:2020). EN ISO 56000:2021
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There are a variety of methods employed for the manufacture of different materials and their usage. Each method require some degree of regulation depending on the type of nature of the activity. EN 17289-3, 2020 is one of the documents that defines the exact method of application for crystal silica.This document specifies how to determine the size-weighted fine fraction (SWFF) as well as the size-weighted fine portion of crystalline silica (SWFFCS) in bulk materials by means of the sedimentation technique by using a liquid-based sedimentation technique.The aim of this document is to permit users to assess bulk materials in terms of their size-weighted fine fraction and crystalline silica content.This document applies to crystalline silica containing bulk material which has been thoroughly studied and validated for the assessment of the size-weighted, fine fraction as well as the crystallized silica.The process of creating a controlling system is made much simpler by the definition of manufacturing methods. If you're interested in reach new markets, we recommend that you invest in international standards for the facility. See the top cen catalog standards en-iso-8307-2018 blog.

Software Engineering Systems - Software Product Quality Requirements Evaluations (Square). Common Industry Formats (Cif) For Usability. Specification For User Requirements (Iso 25065.2019). EN ISO 25065:2020
The most important benefit of a high-end position in the international market is the quality of software. These markets have specific rules which must be adhered to in the present. These rules are contained in documents like EN ISO 25065: 2020.This document provides a uniform framework and uniform terminology for defining the requirements. It defines the industry standard form (CIF) to describe the user's requirements and also includes the elements of content.A specification for user requirements is an official description of a specific set of user requirements that assists in the design of interactive systems.This document defines user requirements as follows. Requirements for interaction between users and systems to produce the desired outcomes (including the requirements and attributes of system outputs and their characteristics) 2. Quality requirements that are related to usage that specify quality criteria in relation to the results of the users' interactions with the interactive software and can be used in conjunction with system acceptance requirements.ISO/IEC 25030 defines quality requirements. One kind of quality requirement is the use-related quality requirements. The elements in specifications for user requirements are designed to be used as part of the documentation that is derived from the activities specified in ISO 9241-210 and from human-centered design processes similar to those found in ISO 9241-220.This document is intended to be used by requirements engineers as well as product managers, business analysts and product owners, as well as anyone purchasing systems through third parties. CIF Series of Standards addresses usability information (as specified by ISO 9241-11 & ISO/IEC TR 25606).Beyond the user-friendly aspect, requirements for usability can include other perspectives, such as human-centred quality that was introduced in ISO 9241-220, and other quality perspectives presented in ISO/IEC 25210, ISO/IEC TS 25011, and ISO/IEC 25030.This document was developed for interactive systems however it can be used in any field. The document is not a guideline for any process, method or lifecycle. It is possible to use the content elements of a user requirement specification in iterative design. This can include the elaboration or evolution of requirements. as in agile development).
Use of this international standard can significantly aid your professional activities. It can also help you structure your current system and offer new opportunities to conquer new markets and scale your business. Have a look at the recommended etsi catalog standards etsi-ts-100-392-19-2-v1.1.1-2019-03 blog.

Health Informatics: Device Interoperability – Part 10201: Point Of Care Medical Device Communication – Domain Information Model (Iso/Ieee 11073/10201:2020). EN ISO/IEEE 11073-10201:2020
Medical devices have parts that can be combined, and they can also discuss completely different technology. EN ISO 11073-10201 / IEEE 11073-10201 2020.The scope of this project is to establish a general object-oriented information model that may be used to organize data and distinguish services utilized in the point-of-care (POC) medical device communication. This project is mostly concerned with acute care medical devices as well as the communication of vital information about the patient.Information technology is increasingly becoming popular in expanding businesses and improving productivity. We recommend that you consider purchasing documents that will standardize their use on a global scale. Have a look at the top cen catalog standards en-17117-1-2018 site.



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