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По умолчанию ISO Standardization Is Essential To Business Development

Part 2-11 - Electrical Equipment For Medical Use: Specific Needs For Basic Safety And Vital Performance In Equipment For Gamma Beam Therapy En 60601-2-11:2015
In some instances, medical equipment could be used to treat a condition but may also cause hazardous negative side consequences. In such a case the use of the equipment is obligatory for decreasing the possibility of occurring negative effects. EN 60601-2-11.2015 is an example of this scenario. The document addresses the safety and essential performance requirements for the gamma beam treatment device, which includes multi-source stereotactic radiation therapy equipment. Manufacturers must adhere to this particular norm from the 60601 series while designing and developing equipment for gamma beam treatment. It specifies tolerance limits that interlocks cannot exceed in order to stop the interruption or termination of radiation. Specifications are available for both type tests specific to the manufacturer. If your manufacturer is using Gamma therapy equipment available, you can get familiar with our standard by visiting the Item website. See the top rated latest-news articles blog site.

Information Technology -- Security Techniques -Code Of Practice To Implement Information Security Controls Based Upon Iso/Iec 27002, For Cloud Services Iso/Iec 27017:2015
Security issues pertaining to information are being addressed in the modern world and are relevant to every person's daily life and in the organizational structure of a business. ISO/IEC 270717 is one of the standards internationally that govern this subject.ISO/IEC 270717-2015 offers guidelines for checking the security of your information that are applicable to the supply or use of cloud-based services. This Recommendation - International Standard offers guidelines and controls for cloud service providers and cloud service customers.There are today many methods for fast transmission of information, we suggest that you know in greater specific detail the method described in this document by clicking on the link on the site and then reading the entire technical parameters. Have a look at the best sist catalog standards sist-en-50121-3-2-2001 info.

Characterization Of Bulk Materials - Determination A Size-Weighted Fine Fraction, And Crystalline Silicon Content - Part Ii Method For Calculation EN 17289-2:2020
There are a variety of components that can be combined to form an entire standard that covers completely different areas. EN 17178-2 is the 2020 part.This document explains how you can calculate bulk materials' size-weighted-fine percentage (SWFFF) as well as its size-weighted fine percentage of crystallized silica (SWFFCS). This document also outlines the assumptions and prerequisites required for this method.The purpose of this document is to allow users to evaluate bulk materials based on their size weighted fine fraction and crystal silica content.Annexe A includes an exact procedure for evaluating the SWFFs for bulk materials diatomaceous. The porosity of the internal and effective density of diatomaceous soil require that the general instructions in this document be altered.This document may be used for crystalline silica containing bulk substances, provided it has been thoroughly verified and tested to establish the weighted size of the finefraction and crystalline silica.To gain a better understanding of the need to follow these standards, it is essential to examine the technical parameters of production standards against the specifications of standards. If you have questions in the implementation of this phase, you can always seek help from experts in the field of international standards. Have a look at the top rated cen catalog tc cen-clc-jtc-19 information.

Mechanical Products - Methodology To The Reduction Of Environmental Impact In The Process Of Designing And Developing Products EN 16524:2020
As new technologies emerge and more air pollution is reported, environmental and safety concerns are constantly evolving. EN 1654: 2020 is a document that could assist in solving this issue.This document describes ways to minimize the environmental impact of product creation and development. It is specifically designed to mechanical products in accordance with 3.1.This approach is especially useful in the process of redesigning existing products. It can be employed to develop new products when you make an accurate understanding of the (virtual reference) product. This approach is for businesses that are using an ecodesign approach to maximise the environmental impact of products throughout their lifecycles.It helps meet certain requirements in ISO 14001, 2015 on the incorporation of environmental aspects in the design of products. This document is targeted at people who are directly involved in the design and development of mechanical products and also managers responsible for defining corporate policies and decisions. The method is intended to help kickstart ecodesign initiatives within organizations as part of a training and continuous improvement process.The document also includes a template companies can use for communicating their environmental approach. This document is not designed to be used to compare the products of different suppliers. This document is not designed to be used for certification purposes.This document is extremely relevant in the 21st-century, so you should consider the possibility of acquiring the document and integrate it into the activities of your business. See the top rated cen catalog standards en-iso-11348-3-2008-a1-2018 blog.

Health Informatics -- Requirements For International Machine-Readable Coding Of The Identifiers On Packages Of Medicines. ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
The amount of regulations and guidelines that regulate the use of these new technologies is increasing , as more are available. EN ISO/ IEEE 11073-10201 is set for 2020. This document is able to be updated due to innovation.This document provides guidelines on the identification and labeling of medicinal products starting from the point of production of the medicinal product packaged to the point at which you can dispensing the medicine. This document outlines best practice for AIDC barcoding solutions that are suitable for use in applications. However, users should take into consideration the requirements for interoperability in coding for other AIDC technologies, e.g. Radio Frequency IdentificationWe strongly suggest that you purchase the latest version if you've previously worked with this documentand remain in the same area of work. Check out the top rated cen catalog tc cen-tc-85-wg-5 blog.

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