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افتراضي ISO Standardization As A Key To The Growth Of Your Business

Part 2 Specific Requirements For Equipment For Short-Waves That Are Safe And Efficient En 60601-2-3:2015
In the medical industry, short-wave treatment is used extensively. Because of this, regulation is crucial. IEC 60601-2-3.2012 specifies the safety requirements as well as the vital performance of short wave therapy equipment. The definition of equipment for short-wave therapy is medical equipment that allows patients to be treated using electric or magnetic fields in a frequency range greater than 13 MHz, but not exceeding 45 MHz. We suggest that you contact Iteh to find out more about the specifics of this document. Have a look at the best sist catalog standards sist-en-1755-2016 review.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Nowadays, a modern management system is crucial to creating a successful business. It is crucial to keep an eye on the rules which govern it. EN ISO 56002:2021 is an illustration of an international standard.This document offers guidance on how to create, implement, maintain, and improve the effectiveness of an innovation management program that can be utilized across all companies. This document is suitable to:A) companies that strive to be sustained successes by developing and demonstrating the ability to successfully manage innovations to attain the desired results.b) Users, customers, and other interested parties who are looking to have confidence in an organization's innovation capabilities.c) organizations and interested parties looking to enhance communication by establishing the common knowledge of what constitutes an innovative management system;d. Training providers in assessment, training or consulting to manage innovation, and innovation management systeme. Policy makers, who strive for greater effectiveness in implementing programs that target companies that have the capacity to innovate, as well as competitiveness as well as the development society.1.2 All the guidance within this document is general and intended to be applicable to:A) All kinds of businesses regardless of their nature size, size or sector. These guidelines aren't just for established organizations. It is important to recognize that both startups and temporary companies could benefit from them.b) Innovation of all kinds, e.g. process, product, service model, method, etc, ranging from incremental to radical.c) any of the methods, e.g. c) All kinds of strategies, e.g., internal and external innovation, market- and technology-based innovation as well as design-driven innovation.It does not provide a detailed description of activities within the organization, instead, it provides guidelines at a the general level. It does not recommend specific tools or strategies for the development of innovation.If you are confused by a few of the modifications in this document, we recommend you consult with an expert to verify whether the standard that is internationally recognized is suitable to be implemented within your company's current structure. Have a look at the most popular clc catalog standards en-50121-3-1-2015 review.

Characterization Of Bulk Materials - Determination Of A Size Weighted Fine Fraction, Crystalline Silica And The Content Of Crystalline Silica Part 3: Sedimentation Method EN 17289-3:2020
There are many ways to use in the production and use of different materials. Each method requires a specific degree of regulation based on the magnitude of the activity. EN 17289-3,2020 is one of the documents that specifies the exact application procedure for crystal silica.This document provides how to calculate the size-weighted portion (SWFF) as well as the fine portion of crystallized silicona (SWFFCS), from bulk materials. It uses the liquid sedimentation technique.This document aims to facilitate users to evaluate bulk material based on their size-weighted crystalline silica and fine fraction.This document is suitable for bulk silica-containing crystalline materials that have been thoroughly studied and verified for the assessment of the size-weighted fine fraction and crystal silica.It is much easier to describe the production process when creating a control panel. If you're planning to increase your market reach we suggest you purchase international standards for your facility. Check out the best clc catalog standards en-61605-2017 site.

Systems And Software Engineering. Software Product Quality Requirements Evaluations And Evaluations (Square) For Software Products. Common Industry Format (Cif), For Usability User Specifications (Iso 25065.2019). EN ISO 25065:2020
Quality of software is the primary factor for making sure that your company is in a position of strength on the international markets. Knowing the rules of these markets can be achieved through reference to international requirements. These requirements are found in documents such as EN ISO 25065 - 2020.This document offers an outline and a consistent language to define the user's requirements. It is a standard industry format (CIF) that specifies the user's requirements. This is both the content and format.A specification of user requirements is an official description of a specific set of user requirements that assists in the creation of interactive systems.This document refers to the user's requirements. They include the following: a) the requirements for interaction between the user and the system in order to reach the desired outcomes (including specifications regarding outputs of the system and attributes) and the) quality standards that pertain to the using the interactive system. These requirements for quality can be used as a basis for system approval.ISO/IEC 25030 establishes requirements for quality. This document defines a specific kind of quality requirement which is the quality requirements related to use. These content elements are designed to form part of documentation resulting in the activities described in ISO 9241-210 and human-centered design processes like ISO 9241-220.This document is designed to serve as a guideline by business analysts, requirements engineers as well as product managers. It can also be used for product owners who are acquiring systems from third-party suppliers. CIF's standards cover usability-related data (as specified in ISO 9241-11 & ISO/IEC TR25060).Beyond accessibility, the requirements of users can include other perspectives like human-centered quality, which is introduced in ISO 9241-220, as well as other quality perspectives presented in ISO/IEC 25210, ISO/IEC TS 25011 and ISO/IEC 25030.This guideline was designed to be used in conjunction with interactive systems. However, it can be applied to other domains. This document does no prescribe any process, method or lifecycle. Iterative development involves the creation and development of requirements (e.g. as in agile development).
The international standard will make your professional activity considerably simpler. It will also aid to structure the existing system and provide new opportunities for expanding your reach in the marketplace and business expansion. See the most popular iso catalog standards iso-astm-51649-2002 blog.

Health Informatics: Standard Communication Protocol For Electrocardiograms That Are Computer-Aided EN 1064:2020
While it was only 10 years ago when medical technology was being introduced all over the globe, this has evolved in recent years. With growing attention paid to human bodies, advancements and development within the medical field is now focused on specific. This industry is responsible to protect the life of humans. Therefore, much attention is paid to security of information. It is regulated by international standards, such as EN 1064:2020.This document defines the specifications for cart-to-host and exchange of specific patient data (demographic as well as recording ...), ECG signals data, ECG measurement, ECG interpretation results). This document details the content and format of the data to be transferred between digital ECG Carts as well as computer ECG Management Systems, in addition to other computer systems in which ECG data is stored.The implementation of this standard will give a significant impetus for the growth of your business in the market of today, which is why we recommend that you familiarize yourself with its details in more detail by clicking on the link to our website. Have a look at the most popular sist catalog standards sist-en-60942-1998-a1-2002 information.



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