10-13-2021, 07:35 PM
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رقم المشاركة : [22]
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ISO Standardization Is A Crucial Element For Development Of Your Business
Part 2 Part 2: Medical Electrical Equipment En 60601-2-3:2015
The medical sector is increasingly utilizing short-wave therapies. Because of this, regulation is so important. IEC 60601-2-3.2012 sets out the safety requirements and fundamental performance of short-wave therapy equipment. Medical equipment that utilizes short-wave radiation therapy for the treatment of patients is defined as any device that exposes patients to magnetic or electric fields that have frequencies of greater than 13MHz, but lower than 45MHz. Iteh is advised to read this document as it has an unspecified specification. Check out the top iec catalog standards iec-60050-713-1998-amd3-2018 info.
Innovation Management - Fundamentals And Vocabulary (Iso 56000 :2020). EN ISO 56000:2021
In some instances, when it comes to technological standards like for instance, the description of the issue of information security the need for explanation documents is created to ensure that people don't misunderstand the meaning of this or that word. EN ISO 56000: 2021, is a good example. This document provides the definitions, basic concepts and principles of innovation and its application in a systematic manner. It can be utilized to:A) Companies that are implementing an innovation management program or conducting assessments on innovation management.B) Organisations that must enhance the effectiveness of their innovation management processesc) customers, customers, and other relevant parties (e.g. suppliers, partners, funders university, investors, and government officials) looking to have confidence in the innovation capabilities of an organization.d. organisations and interested parties who want to improve communication through an agreed-upon understanding of the terminology used in innovation administration;e. providers of training in or assessment of innovation management, and consultancy for it;F) developers of innovation management and related standards.1.2 This document is meant to be used in conjunction with:b. All kinds of innovations, e.g. Innovations of all kinds, including product, service and model. They may be either radical or incremental.c) various types of methods, e.g. Open and internal innovation, market-based, technology- and design-driven innovations.This document outlines the terms that are used in all ISO/TC 279 standards related to innovation management.The standard is packed with important clarifications. We recommend that you go through them thoroughly and cross-check their accuracy with your technological base to make sure that they are the right document to use to promote your business internationally. See the most popular cen catalog standards en-iso-5136-2009 review.
Characterization And Determination Of Bulk Material And Crystal Silica Content. Part 1. General Information And Options Of Test Procedures EN 17289-1:2020
The diversity of manufacturing materials makes it difficult to regulate both locally as well as globally. To ease the entry of companies and organizations into new markets international standards are being created One of them is EN 17178-1: 2020.This document provides the necessary requirements and options for selecting the most appropriate method of testing to determine the size-weighted percentage of crystallized silica and the SWFFCS in bulk materials.This document provides guidelines regarding the preparation of the sample as well as determination of crystallized silica through X-ray Powder Diffractometry (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR).EN 1789-2 is an approach to formulating the size-weighted fine fraction using an estimated range of particle sizes. This is assuming that the distribution of crystalline silica particles in bulk materials is the same. EN 17289-3 describes a liquid sedimentation method to determine the size-weighted fine portion of crystallized silica. Both methods are restricted in their scope and rely on certain assumptions. The procedure in EN 1789-3 could be applied to other components other than CS, if investigated and validated.This document is applicable to crystallized silica with bulk material that has been thoroughly investigated and validated for the assessment of the size-weighted, fine fraction as well as the crystallized silica.If your field of work is in direct contact with any of the materials described in this document, its inclusion in your documentation base for technology can greatly assist in the process of increasing production. Our website will provide more details. See the top rated cen catalog standards en-365-2004 site.
Safety Of Machine Tools - Pneumatic Presses - Part 4. (Iso 160922-4.2019). EN ISO 16092-4:2020
Safety concerns are always one of the most important aspects when creating a regulation system for a manufacturing or company, and that's why there are many of international standards that address this topic, one of them is EN ISO 16092-4:2020.This document, in addition to ISO 16092-1, outlines the safety standards for technical equipment and procedures to be implemented by those who design, manufacture and supply of pneumatic presses which are intended to work cold metal or material partly of cold metal.This document outlines all possible risks that could be a concern for pneumatic presses. It is recommended that they be used according to their intended purpose and in conditions of misuse that are easily predicted by the maker. (See the Clause 4). Every phase of the machine's life-span as described in ISO 12100, 2010, 5.4 are taken into consideration.You can inquire about the technical specifications, and get in touch with us if you're interested to purchase this document. See the most popular cen catalog standards en-14434-2010 blog.
Health Informatics -- Requirements For International Machine-Readable Codes Of Medicinal Product Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
There are additional rules that regulate the use of emerging technologies and reduce risks when they are made accessible. EN ISO 11073/10201 / IEEE 11073-10201 - 2020 is one instance.This document offers guidance on the labelling and identification of medical products beginning with the production of the product to the point at which the product can be disposed of. This document provides the best practices for AIDC barcoding solutions for applications. However, some users might be looking for the interoperability of coding requirements of different AIDC methods, e.g. Radio Frequency IdentificationIf you've utilized a prior version of this document, and are continuing to work in the same field of operation we strongly recommend buying this document that has been updated with recommendations and international rules. See the recommended sist catalog standards sist-en-iso-4869-2-1999-ac-2007 review.
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