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发表于 2021-10-14 00:29:43 | 显示全部楼层

ISO Standardization Is A Key To The Development Of Your Company

Part 2 Specific Requirements For Short-Wave Equipment That Are Safe And Efficient En 60601-2-3:2015
In the medical sector Short-wave treatments are used extensively. This is the reason why regulation of short-wave therapy is essential. IEC 60601-2-3:2012 specifies the requirements for the safety of the fundamentals and essential performance of equipment for short-wave therapy. A device that uses short-wave therapy is any medical equipment used to treat patients exposing them to electric or electromagnetic fields. The frequency range over the device's operation must not exceed 13 MHz and not exceed 45 MHz. As far as the specifications in this document are narrow it is recommended to become familiar with it in a more detailed way with contacting Iteh. See the recommended cen catalog standards pren-16416 info.

Information Technology -- Security Techniques -Code Of Practice To Implement Information Security Controls That Are Based On Iso/Iec 27002, For Cloud Services Iso/Iec 27017:2015
Security issues pertaining to information are being raised in modern society and are important to every person's daily life and in the organizational structure of businesses. ISO/IEC 270717, 2015 is an international standard that governs the issue.ISO/IEC 270717:2015 provides guidelines for information security controls that are applicable to the supply and use of cloud-based services. The guidelines include an additional guidance for implementation for the relevant controls that are outlined in ISO/IEC 27002; - additional controls with implementation guidance that specifically pertain to cloud-based services. This Recommendation  International Standard includes guidelines for implementation and controls for both cloud service providers as well as cloud service users.Since today there are numerous ways to send fast information, we suggest that you understand in greater specific detail the method discussed in this document by clicking on the link to the site and then reading the entire technical parameters. Have a look at the recommended clc catalog standards en-62805-2-2017 info.

Bulk Materials For Characterization - Determination Of Size-Weighted Fine Particles And Crystalline Silica Content Part 1 General Information And The Selection Of Testing Methods EN 17289-1:2020
The variability of the materials used in production significantly makes it difficult to regulate both locally and internationally. International standards are currently being developed to allow organizations and companies to expand their market.This document outlines the requirements and testing options to determine the fine fraction of crystalline silica (SWFFCS) as well as the size-weighted small fraction (SWFF).This document provides guidelines on the preparation of the sample, as well as the measurement of the crystallized silicona with Xray Diffractometry XRD (XRD) as well as Fourier Transform Infrared Spectroscopy FT-IR (FT-IR).EN 1789-2 provides a method to calculate the size-weighted fine fraction from a measured particles size distribution. The method assumes, however that the sizes of the crystalline particles are similar to the bulk material. EN 1789-3 describes a procedure that makes use of liquid sedimentation to calculate the size-weighted fines of crystalline silicon. Both methods are restricted in their scope and rely on certain assumptions. If validated and investigated and analyzed, the EN 17289-3 method could be used to calculate other constituents.This document covers crystalline silica containing bulk material that has been rigorously studied and verified for the evaluation of the size-weighted, fine fraction as well as the crystalline silica.If your field of work is in direct contact with any of the substances mentioned in this document, including it in your technological documentation base will greatly facilitate the process of increasing production. Follow the link to our website for more information. Check out the best cen catalog standards en-326-2-2010 review.

Software Engineering And Systems – Software Product Quality Requirements Evaluation (Square). Common Industry Format (Cif). Usability: User Requirements Specification. (Iso 25065, 2019). EN ISO 25065:2020
Software quality is today the most important factor in ensuring a position of leadership on international markets. To comprehend the rules of these markets, it is essential to know the international standards that must be adhered to in the present. These regulations can be found within documents such as EN ISO 25065 - 2020.The document offers a structure and consistent terminology for describing the requirements of users. It defines the industry standard form (CIF) to describe the user's requirements and also includes the content elements.A specification for user requirements is the formal description of a set user requirements that assists in the development of interactive systems.User requirements, as used in this document, refer to: the following. interactions between users and the system (including requirements system outputs and their characteristics) as well as the second. Quality Requirements for use-related purposes that define the quality requirements for interaction between users and the interactive system. It can be used to determine system acceptance standards.ISO/IEC 25030 establishes requirements for quality. The requirements for quality related to use in this document are a particular type of quality requirements. The information contained in a specifications can be used in documentation resulting from activities in ISO 9241-210 or from human-centred design processes like those in ISO 92421-220.This document is intended for requirements engineers, product managers, product owner, and business analysts who are responsible for acquiring systems from other parties. CIF's standards cover information related to usability (as defined in ISO 9241-11 & ISO/IEC TR25060).Not only can they be used, but so can other perspectives. ISO 9241-220 introduces human-centred characteristics. Additional quality perspectives are provided in ISO/IEC 2510 and ISO/IEC TS 25011.This document was created to be used in conjunction with interactive systems. However, it can be applied to different domains. This document does not recommend any particular approach of lifecycle, process, or method. Iterative development, which involves the creation and development of requirements (e.g. as in agile development).
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Health Informatics -- Requirements Regarding International Machine-Readable Coding Of Medical Product Packaging Identifications ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
The number of regulations and guidelines that govern the use of these new technology is growing as more of them are made accessible. One example of such documents, which is amenable to revision due to new developments and technology is EN ISO / IEEE 11073-10201: 2020.This document offers guidelines for the identification and labeling of medicinal products, starting from the point of production of the packaged product until the point at which you can dispensing the product. This document discusses best practice in AIDC barcoding technologies. The specifications for interoperability in coding for different AIDC technologies can be taken into consideration by users, e.g. Radio Frequency IdentificationIf you've previously worked with this document and are still operating in the same field, we recommend buying the latest version that has updated recommendations. See the most popular cen catalog standards en-iso-10140-3-2010 review.

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发表于 2021-10-14 01:05:43 | 显示全部楼层

ISO Standardization Is An Important Step In Your Business's Development

Part 2-6 Electrical Medical Equipment: Requirements For The Critical Safety And Efficiency Of Microwave Treatment Equipment En 60601-2-6:2015
EN 60601-2-6 2015 is yet another significant document that regulates equipment production and use. It specifies minimum requirements to ensure that microwave therapy equipment is safe to operate. The specific standard is an update to and supplement to IEC 60601-1 (3rd edition 2005, with amend 1in 2012). This second edition cancels and replaces the first edition of IEC 60601-2-6 which was released in 1984. This is yet another reminder that it is important to stay current with new standards that enhance your business' image as well as the productivity of your business's performance. Check out the most popular sist catalog standards osist-pren-4862-2021 review.

Innovation Management - The Basics And Vocabulary. (Iso 56000.2020). EN ISO 56000:2021
Sometimes, documentation is designed to prevent misperception of technical standards like, for instance the concern with information security. An example of this is EN ISO 56000: 2021. This document provides the basic, concepts, and principles for managing innovation as well as the systematic way to implement it. It can be used for:a) Organizations that implement an innovation management strategy or conduct assessment of their innovation management.b. Companies that need to enhance their management of innovative activitiesc. customers, users and other relevant individuals (e.g. To ensure confidence in the company's innovation capabilities, suppliers, partners or funding organizations, investors universities and government officialsd) organizations and interested parties that seek to improve communication by having a shared understanding of the terms used in innovation management.e) Training providers for assessments, training, or consultation on the management of innovation and its systems.F) innovators of innovation management standards and other related ones.1.2 This document is designed to be used by: a) any type of organization, regardless of type, sector, maturity-level or size;b. All forms and kinds of innovation, e.g. Any type of innovation that include product, service and model. They can be either radical or incremental.C. Any kind of approach including. Open and internal innovation and market-based technology- and design-driven innovations.This document describes what terms and definitions are applicable to all ISO/TC 279 innovation management and innovation system standards.It is recommended that you go through this standard in detail. It is also possible to compare them with your technological foundation to ensure you have the right document to help you promote your organization internationally. Check out the best iec catalog standards iec-61496-3-2018 review.

Characterization And Calculation Of Bulk Materials EN 17289-2:2020
One component of the same standard may be used to complement another or even regulate completely various areas. EN 17289-2, 2020 is the second part of the previous standard.This document explains how bulk materials can be used to calculate the size-weighted fraction of fine silica (SWFFF) as well as the fine fraction of size-weighted crystal silica (SWFFCS). This document also provides requirements and assumptions that need to be met in order to ensure the validity of this method.This document is intended to help users evaluate bulk materials in terms of their fine fractions weighted by size or crystallized silica.Annex A provides an illustration of how to evaluate the SWFF in bulk materials made of diatomaceous soil. An Annex A provides specific guidelines for evaluating SWFF of diatomaceous earth bulk materials. This is because of the internal porosity.This document can be used to describe the bulk materials containing crystalline silicona that have been fully examined and validated to assess the size-weighted, fine fraction as well as crystallinesilica.It is crucial to evaluate the technical requirements of production standards as well as the requirements of the individual standards in order to gain a greater understanding of the necessity to apply these standards. If you have questions in the implementation of this stage, you can always seek help from an expert team in the industry of international standards. Check out the best 39.040.99 catalog ics blog.

Safety - Woodworking Machinery - Saws For Construction Sites (Contractors Saws) (Iso 19085-10 – 2018 - Corrected Edition 2019-12) EN ISO 19085-10:2019/A11:2020
Certain standards may have additional features due to technological developments However, the original appearance of a standard doesn't change. EN ISO 1905-10 / 2019/2020.2020-07-20 JF. The CEN Technical Board approved revised Annex ZA through the C132/2020 decision taken on 2020-0708, and the European Amendment to EN ISO 19085-10. European modification is currently in the process of being published.You can contact the iTech team if have any questions after you have read this document. See the recommended iso catalog standards iso-11461-2001 information.

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 other regulations that regulate the use of emerging technologies, and help reduce the risk when they are made accessible. EN ISO11073/10201 IEEE 2020 is an document that are easily modified through innovative developments.This document provides guidelines for the identification and labelling medical products from the time of manufacturing of the medicinal product up to the point at which the product is dispensable. This document offers best practices to use AIDC barcoding solutions. Users can, however, think about the interoperability requirements for different AIDC technology, e.g. Radio Frequency IdentificationIf you've already utilized the previous version and wish to keep operating in the same activity field, we recommend that you update this document with international guidelines and rules. Have a look at the top rated iec catalog standards iec-tr-62652-2010 information.

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发表于 2021-10-15 17:25:05 | 显示全部楼层

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