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افتراضي ISO Standardization Is An Essential Stage In The Growth Of Your Company.

Part 2-11: Safety And Performance Requirements For Electrical Equipment Used In Medical Care En 60601-2-11:2015
Sometimes medical equipment can be used for treatment but at the same time it can cause some harmful effects following. It is essential to use equipment in such situations to reduce the chance of negative effects. EN 60601-2-11.2015 is a document which outlines this kind of scenario. This document focuses on the safety requirements for the gamma radiation therapy equipment. This specific standard, part of the 60601 Series, defines the requirements that must be met by manufacturers when designing and constructing gamma-beam therapy equipment. It sets limits on tolerance to ensure that interlocks are not employed to stop, interrupt or terminate irradiation beyond these limit. Type tests which are performed by the manufacturer or site tests, which are not required to be carried out by the manufacturer are defined for each need. You can access our standard if your company is linked to gamma beam treatment equipment by clicking the link. Have a look at the top sist catalog standards sist-ts-cen-iso-ts-80004-1-2016 review.

Information Technology Security TechniquesCode Of Practice To Establish Information Security Controls Based Upon Iso/Iec 27002, For Cloud Services Iso/Iec 27017:2015
Information security concerns are becoming more and more relevant in our modern-day society. ISO/IEC 27017 is one of the international standards that regulate this topic.ISO/IEC 27017 – 2015 gives guidelines for security checks of information for the use or use of cloud services. This Recommendation International Standard provides guidelines for implementation and controls for both cloud service providers as well as cloud service customers.Today, there are many ways to quickly transmit information. We recommend that you review all the technical parameters and then click the link for more information. See the top rated sist catalog standards sist-en-iso-3016-2019 blog.

Analyzing And Determining Bulk Materials And Crystalline Silica Content. Part 1. Information About The General Aspects And Selections Of Testing Methods EN 17289-1:2020
The vast array of materials used in production complicates regulation both locally, and internationally. International standards are currently being developed to facilitate organisations and companies to enter new markets.This document provides information on the testing requirements and methods that can be employed to determine the size of the fine fraction of crystal silica (SWFFCS), in bulk materials.This document contains guidance regarding the preparation and analysis of crystalline Silica by Xray-ray Diffractometry (XRD) also known as Fourier Transform Infrared Spectroscopy.EN 1789-2 describes a method of getting the size weighted fine fraction based on the measurement of the distribution of particle sizes. This is assuming that the distribution of silica crystals particles in bulk materials is the same. EN 17289-3 describes how to calculate the size-weighted fine percentage of crystalline silicona by using liquid sedimentation. Both methods are limited by assumptions and limitations. If the method is validated and studied, the EN 17289-3 method may be employed to calculate other constituents.This document applies to crystallized silicona that contains bulk materials which have been thoroughly examined and verified to assess the size-weighted, fine fraction as well as crystalsilica.If your business involves the materials mentioned in the description of this document, then its presence in the technological documentation base of your business will significantly assist in expanding production. Follow the link to our website to learn more. Have a look at the top rated clc catalog standards en-60068-2-74-1999 review.

Methodology For Reducing Environmental Impacts In The Design And Development Of Mechanical Products EN 16524:2020
As the latest technologies and air pollution increase also, so are environmental and safety concerns. EN 16524, 2020 is one of the papers that can assist in solving this problem.This document provides a strategy to reduce the environmental impact through product design and development that is tailored to mechanical products as defined in 3.1.This method can be employed for the redesign of existing products, but it could also be applied to new products if the appropriate assumptions are made regarding the original product. This method is used by businesses that adopt an eco-design approach to minimize environmental impact over the course of product life cycles.It meets some of the requirements in ISO 14001 :2015 regarding the integration of environmental factors in the design of products. This document is for those who are involved in the development, design, and maintenance of mechanical devices. The approach is intended as a way to stimulate ecodesign efforts within companies.The template is a great tool to be used by companies in their communications regarding their environmental approach. This document does not allow for the comparison of different products, including those which are similar, from different suppliers. This document is not eligible for product certification.This document is relevant especially for the 21st century. That is why you need to take note of the possibility of getting it , and then integrating it into the activities of your organization. Have a look at the recommended sist catalog standards sist-en-1539-2016 blog.

Health Informatics: Standard Communication Protocol- Computer-Assisted Electronic Cardiac Imaging EN 1064:2020
Although the introductions of new technologies to medicine were slow a decade back however, they have become increasingly prevalent in recent years. The security of human life is the main concern of this business. Information security is an important issue. EN 1064 is 2020 is an example of such international standards.The document outlines the most common guidelines that are necessary to allow cart/to cart and cart/to host interchange of specific patient data. These include data about the patient, their demographics as well as recording information, ...), 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 computers ECG management systems, as well as other computer systems in which ECG data can be storedThis standard can be an extremely effective tool for your company's growth in today's competitive market. This is why we recommend you review the details of the standard by clicking on the link we have on our website. See the recommended cen catalog standards en-12221-2-2008a1-2013 review.



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