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Oanghai091 发表于 2021-9-22 22:21:51
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FrankJScott 发表于 2021-10-12 22:01:27

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FrankJScott 发表于 2021-10-13 23:22:21

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

Part 1-9 Medical Electrical Equipment Safety Requirements For Essential Performance - Collateral Standard. Requirements For Eco-Friendly Design En 60601-1-9:2008
Environment is vital for humans everywhere. Technology is constantly changing and it's crucial to ensure the safety of every new system. The new standards are being created for medical equipment in order to guarantee environmental security. This collateral standard was created to increase the safety of environmental protection for medical electrical equipment. This involves protecting the environment as well as the health of humans from harmful substances, while conserving raw materials and energy and minimizing the production of waste, as well as minimizing the negative environmental effects associated with garbage. The criteria required to achieve this goal must be integrated into every stage of the medical electrical equipment life cycle , starting from the initial stage of specification to the ending of life management. Visit the website for more detailed information about this important document. See the top cen catalog tc cen-tc-69-wg-17 review.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
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Characterization Of Bulk Materials - The Determination Of A Weighted Size Fine Fraction, Crystalline Silica, And Crystalline Silica Contents Part 3 - Sedimentation Method EN 17289-3:2020
Many methods are employed in the process of production and make use of various materials. Each one requires a certain level of regulation that is suitable to the specific activity. EN 17178-3, 2020 is one of the documents that standardizes the precise application method for crystal silica.This document describes how to determine the size-weighted crystalline silica fine fraction (SWFF) as well as the size-weighted fine fraction (SWFFCS), in bulk materials , using an approach to sedimentation that employs the method of liquid sedimentation.This document will enable the users to examine bulk materials in relation to their size-weighted fine fraction and crystal silica content.This document is applicable for bulk silica-containing crystalline materials which have been fully investigated and validated for the evaluation of the size-weighted fine fraction and crystal silica.The specification of production methods greatly eases the process of creating the control system. If you're considering exploring new markets, we strongly suggest to consider purchasing international standards for your plant. Have a look at the recommended sist catalog standards sist-en-61850-8-1-2011-a1-2020 blog.

Methodology To Minimize Environmental Impacts In The Development Of Products And In The Design Of Mechanical Products EN 16524:2020
The issues of safety and environment are constantly evolving with the advent of new technology and pollution from the air emerge. EN 16524 2020 is a document that may help solve this problem.This document provides guidelines on how to lessen the environmental impact of product design and development. It is designed for mechanical products according to 3.1.This methodology can be used to redesign existing products, however it can also work for new products if the necessary assumptions are made regarding the reference product. It can be applied to businesses which integrate ecodesign to lessen environmental impacts in the lifecycle of the product. This includes other aspects such as product performance, quality, price, etc.It helps meet certain requirements of ISO 14001, 2015 on the integration of environmental issues in the design of products. This document is targeted at those directly involved in the creation and development mechanical products. It also targets managers and decision-makers who are responsible for corporate policies and decisions. The method proposed is designed to encourage ecodesign efforts within companies.This document also includes an example template that businesses can use as part of the announcement of their environmental policy. This document is neither intended or suitable for comparing the products (even similar) from different suppliers. This document is not suitable for product certification.This document is vital, especially in the 21st Century. It is therefore important to be aware of the possibility of buying it and introducing it to your activities. Check out the recommended clc catalog standards en-61334-4-512-2002 blog.

Health Informatics -- Requirements Regarding International Machine-Readable Coding Of Medical Product Packaging Identifications ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As more and more technology becomes available, regulations are being created to control their use and reduce risk. EN ISO 11073/10201 / IEEE 11073-10201 2020 is a prime example.This document provides guidelines for identifying and labelling of medicinal substances beginning at the time of manufacturing the packaged medicinal product up to the point of dispensing it. This document outlines the best practices in AIDC barcoding for applications. However, users should consider the coding interoperability requirements for other AIDC technologies, e.g. Radio Frequency IdentificationIf you've previously used a previous version of this document, and are continuing to operate within the same area of work, we strongly recommend purchasing this document that has been updated with guidelines and international regulations. See the recommended aee0a6c9a52e46d49336529991919418 samples 76470 review.

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