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发表于 2021-10-14 00:52:32
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ISO Standardization: A Key To The Development Of Your Company
Part 1-10 Of Medical Electrical Equipment: Essential Safety And Performance - Collateral Standard. The Requirements For Designing Closed-Loop Systems That Are Physiologic En 60601-1-10:2008
Safety of the equipment used in medical facilities is guaranteed by the creation of separate specifications. Standards are created not only for the procedure of use, but also for the production. It is important to be aware of new standards that are being developed in the area of medical equipment. EN 60601-1-10.2008 specifies the requirements for developing (analysis of design as well as verification and validation) a physiologic close-loop controller which is part of a medical closed-loop system for controlling the physiological variables. This collateral standard can be applied to various types of PCLCs, e.g. This collateral standard covers all types of PCLC, which includes those that are linear or non-linear, adaptive, fuzzy and neural. It also applies to closed-loop controllers that set the output variable to change the physiologic variables measured by linking them to the reference variable. If you are interested in this document, contact Iteh. Have a look at the best cen catalog standards fpren-54-30 site.
Innovation Management - The Basics And The Terminology (Iso 56000.2020) EN ISO 56000:2021
Explanatory documentation are sometimes created in order to avoid misconceptions about technical standards such as, for instance concerns with security of information. EN ISO 56000 2021 is an excellent instance. This document outlines the fundamental concepts, vocabulary and fundamentals of innovation management, as well as their systematic implementation. It can be used for:A) Businesses that are in the process of implementing an innovation management program or conducting assessment of their innovation management.b) companies that must improve their ability to effectively manage innovation activities;c. Users, customers, and other pertinent parties (e.g. For confidence in the organization’s capability to innovate suppliers, partners or institutions of funding, investors and other authoritiesd. organisations and those who wish to improve communication using a common understanding for the terminology employed in innovation administration(e) Providers for training in assessments, training, or consultation on the management of innovation and its methods.F. Innovation management standards and standards related to them1.2 This document is meant to be used in conjunction with:b. All kinds of innovations, e.g. product, service, process or method that range from small to radical;C) Any kind of approach, e.g. Both internal and external innovation, as well as technologies, market-based, and design driven initiatives for innovation.This document provides all relevant terms and definitions of the ISO/TC 279 standard for innovation management.The clarifying features listed above are many, so we recommend that all of them be thoroughly scrutinized and compared with the technology foundation of your organization. This will help you increase your company's visibility at an the international level. See the top iec catalog standards iec-60107-5-1992-amd1-1999 information.
Characterization Bulk Materials - Determination Size-Weighted Fine Particles And The Content Of Crystalline Silica - Part 3: Sedimentation Method EN 17289-3:2020
A variety of techniques are employed to make and use various materials. Each one needs a certain amount of regulation, based on the scale of the operation. EN 17289-3 2020 is one document that outlines the precise application method for crystallized silicona.This document provides how to calculate the size-weighted fraction (SWFF) as well as the fine portion of crystalline silicona (SWFFCS) in bulk materials. It uses the method of liquid sedimentation.This document is intended to help users evaluate bulk materials in relation to their size-weighted fine fraction or silica crystalline.This document covers crystallized silica that contains bulk substances which have been fully assessed and validated for the evaluation and size-weighted fine fraction.The process of creating a control system is made much simpler by the definition of the production processes. If you're interested in reach new markets We suggest that you invest in international standards for the facility. See the most popular sist catalog standards sist-en-12881-1-2014 information.
Mechanical Products - Methodology For Reduction Of Environmental Impacts In The Process Of Designing And Developing Products EN 16524:2020
The issues of safety and environment are constantly evolving with the advent of new technology and air pollution emerge. One of the documents offering a solution to this problem is EN 16524: 2020.This document outlines a method to minimize the environmental impact of production and design. It is applicable to only mechanical products as detailed in 3.1.This methodology is well-suited to redesigning an existing product. If the assumptions concerning a virtual reference product are established, the technique can also used to design an entirely new product. This is a method for companies who have decided to adopt an ecodesign approach in order to optimize environmental impact throughout the entire lifecycle of the product. The approach also considers different aspects of the product, like functionality, cost as well as the quality.It fulfills some of the specifications of ISO 14001 :2015 regarding the integration of environmental factors in product design. This document is for those who are directly involved in the creation and manufacturing of mechanical products. The methodology proposed is designed to kick-start ecodesign initiatives within organizations as part of a training and continuous improvement process.A template is also included in this document that companies can use to explain their environmental strategy. This document is neither intended to be used for comparison of products (even similar) from different suppliers. This document is not designed or suitable for certification purposes.This document is especially relevant for the 21st century. This is the reason why you should investigate the possibility of obtaining it and how you can incorporate it into your work. Have a look at the recommended sist catalog standards sist-en-13718-1-2015 info.
Health Informatics - Standard Communication Protocol - Computer-Assisted Electrocardiography EN 1064:2020
While the introduction of new technology in medicine was slow in the past but they have become more prevalent in recent years. The safety of human lives is the primary concern of this business. Information security is therefore an essential concern. EN 1064 is 2020 is an example of such international standards.This document defines the most common guidelines that are necessary to allow cart/to cart and cart/to host exchange of particular patient information. This includes data on the patient, their demographics as well as recording information, ...), ECG signal information, ECG measurement results, and ECG interpretation. This document describes the structure and contents of the data that will be transferred between electronic ECG carts, computers ECG management systems, and other computer systems that can store ECG data.This standard will assist you build your business on the modern market. To learn more follow this link. Check out the top iec catalog standards iec-61434-1996 site.
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