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发表于 2021-8-11 00:31:43 | 显示全部楼层 |阅读模式
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发表于 2021-10-4 22:56:35 | 显示全部楼层

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发表于 2021-10-13 23:00:39 | 显示全部楼层

ISO Standardization Is Key To Business Development

Part 2-11: Safety And Performance Requirements For Medical Electrical Equipment En 60601-2-11:2015
Sometimes, medical devices may be utilized in the treatment of a condition. But they can cause serious adverse side effects. Equipment is required in these instances to decrease the likelihood of any negative side effects. EN 60601-2-11.2015 offers an example of this document. The document deals with safety basics and fundamental performance requirements of gamma therapy equipment. This particular standard, from the 60601 serie, sets out requirements that manufacturers must adhere to when creating and designing gamma radiation therapy equipment. It sets limits on tolerance to make sure that no interlocks will be employed to stop, interrupt or stop irradiation that exceeds these limit. For each requirement there are particular requirements for type tests and site tests. The standard we offer is open to manufacturers who have the gamma radiation therapy equipment. Have a look at the most popular cen catalog standards en-1502-2020 review.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
An effective management system is crucial to developing a profitable organization today. This is why it's so important to pay attention to the legal documents that govern it from the beginning to the last stage. EN ISO 56002 will be in 2021.This document provides guidelines for the establishment, implementation, maintenance, and continual improvement of an innovation management system for use in every organization that is established. It is applicable to:A) companies that strive to be sustained successes by developing and demonstrating the ability to manage effectively innovations to get the results they want.b. Users, customers or any other parties looking to be confident in the capability of the business to innovate.c. Organizations and interested individuals looking to improve communication via a common understanding the characteristics of an innovation management system.d. Providers of training in or evaluation of innovation management, or consulting for it.e. policymakers seeking to improve the efficiency and effectiveness of support programs aimed at innovation capability and competitiveness of companies and development in society.1.2 All the guidance within this document is general and is designed to be applicable to:a. Any type of organization, regardless of size, industry, type, or. While the guidelines are intended primarily for established organizations however, they are applicable in any or all cases for start-ups as well as temporary companies.b. All kinds of innovations, e.g. Innovations of all kinds that include product, service and process.c. all methods, e.g. Open and internal innovation technologies, market-based, user- and design-driven innovative activities.The document doesn't detail specific activities in an organization It only offers guidance at the general level. It doesn't include any requirements, tools or strategies that could be applied to develop new ideas.If you're not sure about some of the changes made in this document we suggest you speak with a specialist to confirm whether the international standard is appropriate to be implemented in your organization's existing structure. Check out the top rated cen catalog standards en-15611-2020-pra1 blog.

Characterization Of Bulk Materials - Determination Size-Weighted Fine Particles And Crystalline Silica Content – Part 1: General Information And Choice Of Testing Methods EN 17289-1:2020
The diversity of the materials used in production significantly makes it difficult to regulate both locally as well as globally. International standards are currently being developed to ease the process for organisations and companies to access new markets.This document outlines the criteria to determine the size-weighted fine fraction (SWFF) as well as the size weighted fine fragment crystalline silica (SWFFCS).This document offers guidelines on the preparation and determination of crystalline Silica by Xray-ray Powder Diffractometry (XRD) also known as Fourier Transform Infrared Spectroscopy.EN 1789-2 is a method of formulating the size-weighted fine fraction based on an estimated distribution of particle sizes. This assumes that the distribution of silica crystals particles in bulk material is the same. EN 1789-3 describes the liquid sedimentation process to calculate the size weighted fine silica fraction of crystal. The two methods are based on a number of limitations and assumptions that are described in EN 17289-2 and EN 17289-3 and EN 17289-3, respectively. The EN 17289-3 method could be applicable to other constituents that are not CS if confirmed.This document is suitable to bulk crystalline silica materials which have been fully examined and verified for analysis of the size-weighted fine fraction and crystal silica.If your industry comes into contact with the material described in the description, then it can be a huge help in scaling up production. Visit our website to find out more. Have a look at the recommended sist catalog standards sist-en-17199-3-2019 information.

Machine Tools Safety Presses - Part 4: Safety Requirements For Pneumatic Presses (Iso 16092-4:2019) EN ISO 16092-4:2020
Safety issues are always one of the most important aspects when creating a regulation system for a manufacturing or company, and that's why there is a wide range of international standards affecting the issue, one of which is EN ISO 16092-4: 2020.This document is in addition to ISO 16092-1. It provides the safety measures for technical use and the requirements to be followed by anyone involved in designing or manufacturing pneumatic presses that are meant to work with cold or partially cold metal.This document addresses all hazards that could affect pneumatic presses when employed in line with their intended use and under conditions of misuse which are reasonably predicted by the manufacturer (see Clause 4) All phases, as per ISO 12100:2010, 5.4 are considered.If you're interested in purchasing this document, simply visit the link to get all the technical details. Contact the team to answer any queries. Check out the most popular iso catalog standards iso-dis-24294 blog.

Health Informatics – Device Interoperability Part . 20701 Communication At The Point Of Care Using Medical Devices - Service-Oriented Medical Device Exchange Technology (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
The use of communication technologies is across many fields, not just those directly connected to this field but also in the medical industry. Since the introduction of technology for the operation of different medical devices is a complex process and involves the overhaul of existing systems, international documents are being created to ease these processes, one of them is EN ISO 11073-20701:2020.
This standard is an architecture for medical devices that is service-oriented and Communication Protocol Specification for distributed Systems of Point-of-Care(PoC), medical devices, and medical IT systems that have to exchange data and manage PoC networked medical devices. It defines the functional elements, their communication relations and binding of components and communication relations to protocol specifications.The document is specific and has been narrowly profiled. We recommend that you study the technical aspects of this document and speak with managers who are experts in international document selection. Check out the most popular cen catalog standards en-12309-7-2014 blog.

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