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Part 1 Part 1: Medical Electrical Equipment General Safety Requirements And The Essential Performance – Collateral Standard: Electromagnetic Disturbances. Requirements, Tests En 60601-1-2:2015
Specification of medical equipment demands specific knowledge and a broader design. Each medical system is subject to its own specifications. This document covers the essential safety and performance for Medical Equipment (ME), and ME Systems that are exposed to electromagnetic disturbances. The first section of the standard will give an overview of the safety requirements in the use of medical equipment. Check out the recommended [url=https://standards.iteh.ai/catalog/standards/sist/c1ace23e-bc42-4446-bf92-eaa5d3bf2df1/sist-en-61850-7-3-2011]sist catalog standards sist-en-61850-7-3-2011[/url] site.
Innovation Management — Basics And Vocabulary (Iso 56000 :2020). EN ISO 56000:2021
Explanatory documentation are sometimes created in order to avoid confusion about technical standards, like for example, the issue regarding security of information. EN ISO 56000, 2021 is an example. This document provides the basic concepts, terms, and principles of innovation management and their methodical implementation. It can be used to:A) Organizations that have implemented an innovation management system;B) Organizations that need to increase the effectiveness of their innovation management activitiesc. users, customers, and other relevant parties (e.g. Suppliers, partners funding organizations, investors, universities or public authorities, etc.) who seek to be confident in the capabilities of innovation and performance of an organisation.d. Organizations and other interested parties who want to enhance communication by establishing a common understanding about the terms used to describe innovation managementE) Providers of training, assessment or consulting on the management of innovation and its processes.F. Developers of innovation management standards and other related standards1.2 This document will apply to:b) any kind of innovation, e.g. process, product, service models and methods all types of innovations, from incremental to radical;c) All types of approaches, e.g. c) all types of methods, e.g., internal and external innovation, market-based technology and design-driven innovations.This document defines all applicable terms and definitions to the ISO/TC 279 standard on innovation management.Because there is a vast number of clarifying elements in this standard, we advise to study the entire document and compare them with the technological base of your organization to be sure that it's this standard that can help you effectively manage the promotion of your organization at the international level. See the top [url=https://standards.iteh.ai/catalog/standards/cen/f10807b2-d529-4c46-853d-065561af560f/en-iso-17225-4-2021]cen catalog standards en-iso-17225-4-2021[/url] site.
Characterization Of Bulk Material — Determination Of A Size Weighted Fine Percentage Or Crystalline Silica Content — Part I: Basic Information And Selection Of Test Methods EN 17289-1:2020
Regulations are complicated both locally and internationally because of the wide range of production materials. To ease the entry of organisations and companies into new markets International standards are being created among them EN 17289-1:2020.This document provides information about the requirements and test methods that can be employed to determine the size of the fine portion of crystal silica (SWFFCS), in bulk materials.This document contains guidance regarding the preparation and analysis of crystalline Silica by Xray-ray Powder Diffractometry (XRD), or Fourier Transform Infrared Spectroscopy.EN 17289-2 refers to an approach to formulating the size-weighted fine fraction using an estimated range of particle sizes. This assumes that the distribution of crystal silica particles in bulk materials is the same. EN 1789-3 describes the procedure for liquid sedimentation to calculate the size-weighted fine portion of crystal silica. The two methods are based on a number of limitations and assumptions, which are outlined in EN 17289-2 and EN 1789-3, respectively. If validated and investigated, the EN 17289-3 method can be utilized to calculate additional constituents.This document may be used to evaluate bulk crystalline silica materials, provided that it has been thoroughly researched and verified for the evaluation of size-weighted fine fragments as well as crystalline silica.The technological documentation of your company will be greatly aided if your activity comes in contact with the information contained in this section. For more information, you can follow the link to our website. See the most popular [url=https://standards.iteh.ai/catalog/standards/sist/c4af469c-3d53-427d-acc1-c92220cd4746/sist-en-iec-60384-17-2019]sist catalog standards sist-en-iec-60384-17-2019[/url] info.
Safety Of Machine Tools — Pneumatic Presses — Part 4. (Iso 160922-4.2019). EN ISO 16092-4:2020
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Health InformaticsInteroperability Of Devices. Part 10201. Point-Of-Care Medical Device Communications. Domain Information Model. (Iso/Ieee 11073-10201:2020). EN ISO/IEEE 11073-10201:2020
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