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افتراضي ISO Standardization Is Crucial To The Development Of Your Company

Part 1 Part 1-6: Safety And Performance Requirements For Medical Electrical Equipment. Collateral Standard: Usability En 60601-1-6:2010
At the same time, new technologies are creating rapid progress in the use and production of electronic medical equipment. The scale of production is growing and the demand of these devices is growing. EN 60601-1-6.2010 describes a method by which a manufacturer can examine, define the design, validate and test the usability of medical electrical equipment. This process of usability engineering evaluates and minimizes risks arising from usability issues that are associated with proper usage. If you are employed in the production of medical equipment, it is important that you know this standard. See the top information-technology articles blog info.

Innovation Management – Basics And Vocabulary (Iso 56000.2020) EN ISO 56000:2021
Explanatory papers are sometimes required for technical standards. These documents, for example provide information on information security. EN ISO 56000, 2021 is an example. This document outlines the fundamental concepts, vocabulary and fundamentals of innovation management and their systematic implementation. It can be used to:A) Businesses that are in the process of implementing an innovation management strategy or conducting assessments on innovation management.b) Organisations that must increase the efficiency of their innovation-related management practicesc) customers, users and other relevant parties (e.g. Suppliers, partners and institutions for funding, investors as along with universities and public officials who are looking to have confidence in the innovation capabilities of the company.d) organizations and interested individuals who wish to improve communication via a shared understanding of the vocabulary that is used in innovation managementE. Providers of education in, assessment, or consultancy for innovation management and system-wide innovation managementF) The developers of innovation management and related standards1.2 This document can be used to include. Any type of organization regardless of type and maturity level, sector or size.b) any kind of innovation, e.g. There is the possibility of having a product, service or model.C. All approaches, e.g. Internal and external innovation, and technological, market, and design driven initiatives for innovation.This document defines the terms and definitions that apply to all ISO/TC 279.-developed standards for management of innovation and management systems.There are many clarifying elements within this standard. We recommend to carefully read them and then compare them with the technological foundation of your company to ensure that the document will be able to enable you to take your business to the highest possible level. Have a look at the top iso catalog tc iso-tc-59-sc-13-wg-8 information.

The Characterisation Of Bulk Materials - Determination Of An Amount-Weighted Fine Fraction, And Crystalline Silica Content - Part 3: Sedimentation Method EN 17289-3:2020
Numerous methods are employed for the manufacture of different materials and their application. Each one requires a different level of regulation depending on the magnitude of the operation. One of the documents that standardizes the specific application method for crystalline silica is EN 17289-3: 2020.This document will explain how to determine the size-weighted crystalline silica fine fraction (SWFF), and the size-weighted fine fraction (SWFFCS), for bulk materials by using an approach to sedimentation that employs a liquid sedimentation technique.The goal of this document is to enable users to evaluate bulk materials with regard to their fine fractions weighted by size and the content of crystalline silica.This document can be used for crystalline silica containing bulk materials which have been fully investigated and validated for the evaluation of the size-weighted fraction and crystal silica.It is much easier to define production methods when building the control panel. If you're interested in expanding your market share We recommend that you buy international standards for your facility. Check out the top cen catalog standards en-1355-1996 review.

Machine Tools Safety – Safety For Presses - Part 4: The Safety Requirements Of Pneumatic Presses. (Iso 16092-4.2019). EN ISO 16092-4:2020
Safety issues are always most important aspects when creating a regulation system for a manufacturing or company, and that's why there are a large number of international standards that address the issue, one of which is EN ISO 16092-4: 2020.This document is a supplement to ISO 16092-1. It outlines the technical safety measures and guidelines to be adhered to by anyone involved in designing, manufacturing, and supplying pneumatic presses that are meant to work with cold or partially cold metal.This document details all hazards that could impact pneumatic presses if they are not operated in the manner intended or in circumstances of misuse that are reasonably anticipated by the manufacturer (see Clause 4-). These are all the phases defined in ISO 12100 :2010, Section 5.4.If you are interested, click the link on our website to access the full technical specifications. Also, contact the team with any questions or clarifications. Check out the top cen catalog standards pren-1013 site.

Health Informatics - Standard Communication Protocol - Computer-Assisted Electrocardiography EN 1064:2020
It was only just a decade ago when technology entered the medical field the pace of innovation and development have been speeded up in the last few years. Information security is a crucial aspect of this field because it is responsible for human safety. This is the reason why EN 1064:2020 is an international standard.This document describes the most common standards for cart-to-host and cart-to-cart interchange of particular patient data (demographics and recording), ECG Signal data, ECG measurements, ECG interpretations, results, etc. This document outlines the structure and content that will be transferred between digital ECG carts, computer ECG management system systems, and other computer systems that be used to store ECG data.This standard will assist you to develop your company to compete in the market of today. To find out more follow this link. Check out the top cen catalog standards en-12014-7-1998 review.



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