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افتراضي ISO Standardization Is An Essential Element In Your Business's Growth

Part 1-10 Of Medical Electrical Equipment: Essential Safety And Performance - Collateral Standard. The Requirements For Designing Closed-Loop Physiologic Controllers En 60601-1-10:2008
The safety of medical equipment is guaranteed by the development of distinct details. Standards are not just intended for manufacturing but also for the use. This means that awareness of the latest standards in the area of medical equipment is on the same level as standardization for general purposes. EN 60601-1-10.2008 specifies the specifications for the development (analysis and design), verification and validation of an physiologic closed loop controller. The controller is utilized in a closed loop physiologic control system in medical electronic equipment as well as medical systems to regulate a particular physiologic parameter. This collateral standard covers all types of PCLC, such as those that are linear or non-linear, flexible, and neural. Also, it applies to closed-loop controllers which set the output variable in order to alter the physiologic variables measured by connecting them to the reference variable. Iteh is available to address any questions. See the best clc catalog standards en-iec-60068-2-85-2019 information.

Information Technology -- Security Methods - Code Of Practice For Information Security Controls Based Iso/Iec 27002 In Cloud Services Iso/Iec 27017:2015
Information security concerns are becoming more and more relevant in the modern world. ISO/IEC 27017, 2015 . is an international standard which regulates this subject.ISO/IEC 27017:2015 gives guidelines for the security of information applicable to the provision and use of cloud-based services by providing further guidance on implementation for the relevant controls that are outlined in ISO/IEC 27002; - additional controls and implementation guidelines that specifically pertain to cloud-based services. This Recommendation International Standard includes controls and implementation guidance both for cloud service providers as well as cloud service users.There are many options for quick information transmission today. We suggest you go through the hyperlinks on this website to see all technical details. Check out the best clc catalog standards en-60745-2-19-2005 blog.

Characterization Of Bulk Materials - Determination A Size-Weighted Fine Fraction And Crystal Silica Content - Part 1: General Information And Choice Of Testing Methods EN 17289-1:2020
Variability in manufacturing materials makes it difficult to regulate both locally and globally. International standards are currently being created to facilitate companies and organizations that want to access new markets.This document describes the specifications and alternatives for choosing the best test method to determine the size-weighted fraction of crystalline silica and the SWFFCS in bulk materials.This document provides guidelines for the preparation of the sample and the determination of crystallized silica through X-ray Powder Diffractometry (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR).EN 1789-2 explains how to determine the size-weighted percentage of fine particles based on a measured size distribution. It is based on the assumption that the size distribution of the crystal quartz particles is exactly the same as those of other particles in bulk materials. EN 1789-3 describes a liquid sedimentation method for determining the size-weighted fine fraction of crystalline silica. Both methods are limited in scope and require certain assumptions. If validated properly it is possible that the EN 17289-3 methodology can apply to different constituents.This document may be used for bulk silica-containing crystalline materials, provided that it has been thoroughly researched and verified to permit the evaluation of size-weighted fine fragments as well as crystalline silica.The presence of the technology documentation base will help to increase production levels when your industry is directly in contact with the materials described in the document. For more detailed information you can go to our website. Check out the top rated cen catalog standards cen-tr-16410-2012 review.

Methodology For Reducing The Environmental Impact Caused By Product Design And Development Of Mechanical Products EN 16524:2020
As new technologies and air polluting emerge the environmental and safety issues change. EN 16524: 2020 is one document that offers an answer.This document outlines a strategy to minimize environmental impact by product development and design. It is applicable to mechanical products, as described in 3.1.This method is especially well-suited to redesign an existing product. However, it can be used to design new products if assumptions about the reference product are constructed. This method is used by companies who adopt an eco-design approach to minimise environmental impact throughout the life of their product.It also meets certain requirements in ISO 14001 2015 regarding the incorporation of environmental considerations into the design of products. This document addresses people involved in the development, design, and maintenance of mechanical devices. The approach is intended as part to incite the companies to engage in ecodesign.The template could be utilized by companies as part of their communications regarding their environmental approach. This document is not designed to permit you to compare the products of different suppliers. The document isn't intended to be used for certification of products.This document is especially relevant in the 21st century and you must think about the possibility of purchasing it and incorporate it into the business activities of your organization. See the recommended sist catalog standards sist-en-10288-2003 information.

Health Informatics -Standard Communication Protocol Computer Assisted Electrocardiography EN 1064:2020
While it was only 10 years ago when medical technology was being presented all over the globe, this has changed in recent years. Due to the increasing attention being paid to the human body, innovations and progress in the medical field are now centered in particular. Because this industry is responsible to the safety and security of human life, a lot of attention has been given to security of information. This regulation is EN 1064, 2020.The document outlines the common standards that are needed for the cart/to-cart and cart/to-host exchange of patient-specific data. This includes information about the patient, their characteristics and recording details, ...), ECG signal information, ECG measurement results, and ECG interpretation. This document defines the contents and structure of the information which is to be interchanged between electronic ECG carts and computer ECG management systems, and other systems on computers where ECG data is stored.This standard can help you build your business in the current market. To find out more, click the link. See the best iec catalog standards iec-63013-2017 blog.



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