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发表于 2021-8-21 10:51:43 | 显示全部楼层 |阅读模式
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发表于 2021-9-28 23:51:50 | 显示全部楼层

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发表于 2021-10-14 00:46:38 | 显示全部楼层

ISO Standardization Is A Key To The Growth Of Your Business

Part 2-11 - Medical Electrical Equipment: Specific Specifications For Safety Requirements And Essential Performance In Equipment For Gamma Beam Therapy En 60601-2-11:2015
In some instances, medical equipment could be utilized to treat. However, it could be dangerous and have negative consequences. In order to minimize the possibility of negative outcomes, equipment should be used in such situations. One document that defines this is EN 60601-2-11:2015. The document is about the essential safety of Gamma radiation therapy equipment. This particular standard is part of the 60601 series. It specifies the rules that manufacturers must adhere to when developing and fabricating the gamma beam therapy equipment. It outlines tolerance limits to which interlocks are required to end or stop irradiation, in order to prevent an unsafe condition. The standards cover types and site tests as well as tests performed by the company that manufactures. It is possible to access our standard if your company is connected to gamma beam treatment equipment by clicking the link. See the top rated cen catalog standards cr-14377-2002 site.

Information Technology -- Security Methods -Code Of Practice For Information Security Controls, Based On Iso/Iec 27002 For Cloud Services Iso/Iec 27017:2015
Information security issues become more important in our modern-day society. ISO/IEC 270717 is one of the standards internationally that govern this topic.ISO/IEC 27017:2015 offers guidelines for information security controls that can be used to provision and use cloud services. It provides an additional set of guidelines for implementation to ISO/IEC 27002 controls; - additional controls that have specific guidance for implementation. This Recommendation  International Standard provides the controls and guidelines for implementation for cloud service providers as well as cloud service customers.Since today there are a large number of ways to speed up the transmission of information, we suggest that you clarify in more specific detail the method discussed in this document by clicking on the link to the site and then reading all the technical details. Have a look at the top rated cen catalog standards cen-tr-16396-2020 site.

Characterization Of Bulk Materials - Determination Of A Size Weighted Fine Fraction, And Crystalline Silicon Content - Part Ii Method Of Calculation EN 17289-2:2020
A number of parts can be combined into an entire standard that covers completely different areas. EN 17289-2 is the 2020 part.This document describes the determination of the size-weighted fine portion (SWFF) as well as the size-weighted fine fraction of crystallized silica (SWFFCS) in bulk materials using calculation. The document also lists the assumptions and prerequisites required for this method.The goal of this document is to allow the users to examine bulk materials based on their size weighted fine fraction as well as crystalline silica content.A specific procedure for the assessment of the SWFF for diatomaceous earth bulk materials is given in Annex A. Annexe A provides a distinct method to evaluate the SWFF for diatomaceous-earth bulk materials.This document applies to the bulk silica and crystalline silica which have been thoroughly studied and verified for the evaluation of the size-weighted fine fraction or the crystalline silica.To gain a better understanding of the importance of the standards in question, it's vital to examine the technical parameters utilized in standards for production with the requirements of the specific standards. Experts in the field of international standard can help you with any questions about the application of the stage. Have a look at the best iso catalog standards iso-20730-1-2021 blog.

Software Engineering And Systems. Software Product Quality Requirements And Evaluation (Square). Common Industry Format For Usability (Cif). Specification For User Requirements Specification (Iso 25065.2019). EN ISO 25065:2020
To achieve an advantage on the global market it is vital that they have software of the highest quality. There are specific rules for these markets that must be followed currently. These requirements can also be found in documents such as EN ISO 25065, 2020.This document provides an outline and a consistent language for defining user requirements. It defines the industry standard format (CIF), which is used to specify the user's requirements. This includes the content elements and the manner of expressing those specifications.A specification for user requirements is the formal description of the user's requirements, which aids in the design and evaluation of usable interactive systems.In this document, user requirements refers to interactions between users and systems that are required for achieving intended outcomes (including requirements for system outputs and their attributes) as well as) quality-related requirements for use that define the quality requirements that are associated with the results of users interacting with the system via interactive interface and may be used to determine the level of acceptance for the system.ISO/IEC 25030 specifies quality requirements. The requirements for quality related to use in this document are a particular type of quality requirement. These elements are intended to be part of documentation which will lead to the actions that are described in ISO 9241-210 as well as human-centred design processes such as ISO 9241-220.This document can be utilized by product managers, business analysts and product owners as well as people who acquire systems from third party suppliers. The CIF series of standards covers information on usability (as specified in ISO 9241-11 as well as ISO/IEC TR 25060).Users may also require usability. This is in addition to the quality-oriented perspectives that are provided in ISO 9241-220.This document was initially designed for interactive systems. But it could be used for all types of domains. This document does NOT prescribe any method, lifecycle or procedure. Iterative development involves the creation and development of requirements (e.g. as in agile development).
The use of the international standard will greatly improve your professional work and also help to create a structure for your current system, opening up new possibilities for capturing new markets and scaling your business. Check out the most popular 71-120-10 catalog ics blog.

Health Informatics -- Requirements To International Machine-Readable Codes For Medical Product Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
There are additional regulations that regulate the use of emerging technologies and minimize risks when they are made accessible. EN ISO11073-10201 is set to be in 2020. This document can be revised in response to technological advancements.The document contains guidelines regarding the identification and labelling of medicinal items starting from the time they are made to the point when they are dispensed. This document provides guidelines to use AIDC barcoding solutions. But, it is important to take into consideration the interoperability requirements of other AIDC technologies such as RFID. Radio Frequency IdentificationWe suggest that you purchase the latest international rules and guidelines if you are using a previous version. Have a look at the top cen catalog standards en-13144-2018 blog.

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