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قديم 07-26-2021, 12:24 AM   رقم المشاركة : [11]
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قديم 09-24-2021, 02:50 AM   رقم المشاركة : [12]
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قديم 10-04-2021, 02:21 AM   رقم المشاركة : [13]
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قديم 10-13-2021, 06:59 PM   رقم المشاركة : [14]
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Medical Electrical Equipment - Part 1-9: General Requirements For Basic Security And Essential Performance Collateral Standard Requirements For Environmentally Conscious Design En 60601-1-9:2008
The environment is the foundation of human existence. Technology is constantly evolving but the primary thing to focus on is keeping any new system safe. That's why there are new standards for medical equipment, which govern the environment. The goal of this additional standard is to increase the environmental impact for the entire range of medical equipment, including all stages of the product life cycle including: - specification of the product design; manufacturing and distribution; logistics, sales installation, sales as well as end of life management. This involves protecting the environment as well as human lives from hazardous substances, while conserving natural resources and energy, minimizing the amount of waste created, and minimising any adverse environmental effects. The criteria required to achieve this goal should be incorporated into every stage of the medical electrical equipment life-cycle, from the stage of specification through to end of life management. Visit this site to learn more information about this vital document. Have a look at the most popular sist catalog standards sist-en-iso-7886-4-2019 review.

Innovation Management Tools And Methods For Innovation Partnership – Guidance (Iso 56003-2019) En Iso 56003:2021
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The vast array of production materials creates a challenge for regulation locally and internationally. International standards are being developed to ease the process for organisations and companies to enter new markets.This document provides information about the testing requirements and methods that are used to determine the size of the fine portion of crystal silica (SWFFCS), in bulk materials.This document also provides guidance on how to prepare the sample, and the determination of crystallized silicona with Xray Diffractometry XRD (XRD) and Fourier Transform Infrared Spectroscopy FT-IR (FT-IR).EN 17289-2 describes how to calculate the size-weighted fraction of fine particles using an estimated size distribution. It assumes the particle size distribution for crystalline quartz particles is identical to the distribution of other particles in the bulk material. EN 17289-3 provides a method which uses liquid sedimentation to determine the size-weighted fines in crystalline silica. Both methods are based upon several limitations and assumptions, which are listed in EN 17289-2 and EN 1789-3 and EN 17289-3, respectively. If the method is validated and studied and analyzed, the EN 17289-3 method can be employed to calculate other constituents.This document is applicable to crystallized silicona that contains bulk materials that have been thoroughly studied and validated to assess the size-weighted, fine fraction as well as crystalsilica.If your business is in contact with the subject matter described in this document's description, its inclusion in the documentation base for technology of your company will facilitate the process of increasing production. Visit our website to find out more. Check out the best sist catalog standards sist-en-iec-60601-2-50-2021 info.

Software Engineering And Systems - Software Product Quality Requirements And Evaluation (Square). Common Industry Format For Usability (Cif). User Requirements Specifications (Iso 25065.2019). EN ISO 25065:2020
The quality of software today is the most significant advantage to occupying a leading position in the global market. These markets have specific rules that must be observed currently. These requirements can also be found in documents such EN ISO 25065, 2020.This document offers a consistent framework and terminology for defining user requirements. It specifies the common industry format (CIF) for a user requirement specification including the content elements and the format to express the specifications.A specification of user requirements is a formal description of a specific set of user requirements that aids in the design of interactive systems.This document refers to the requirements of users. They include requirements for interaction between the user and the system (including) requirements to facilitate interaction between the user and the system in order to reach the desired outcomes (including requirements regarding system outputs and attributes); and the) quality requirements related to using the interactive system. These quality requirements can be used as criteria for system approval.ISO/IEC 25030 introduces a concept of quality requirements. These are the types of requirements that are quality-related. The elements that constitute a user requirement specification are intended for use in documentation resulting both from activities listed in ISO9241-210 and human-centered design methods such as ISO9241-220.This document is designed to be used by requirements engineers and product managers, business analysts and product owners and others purchasing systems through third parties. The CIF series of standards focuses on information related to usability (as defined in ISO 9241-11 and ISO/IEC TR 25060).In addition to usability, user requirements can include other perspectives, such as human-centred quality introduced in ISO 9241-220, and other quality-related perspectives that are presented in ISO/IEC 25210, ISO/IEC TS 25011, and ISO/IEC 25030.This document was initially designed to be used in interactive systems. But it can be applied in all domains. This document does NOT prescribe any particular method, lifecycle or procedure. The user requirements specification's content is a good starting point for iterative development. This can include the formulation changes, development and revisions to requirements. as in agile development).
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Health Informatics: Device Interoperability – Part 10201: Point Of Care Medical Device Communication – Domain Information Model (Iso/Ieee 11073/10201:2020). EN ISO/IEEE 11073-10201:2020
Documents related the use of medical devices are identical to the other standards. There are many parts that complement one another and even discuss completely different technologies. EN ISO11073/10201 IEEE: 2020.The goal of this research is to establish a general object-oriented information model that can be used to structure information and identify services used in the point-of-care (POC) medical device communication. The project's scope is primarily focused on medical devices for acute care as well as the information for communication that is derived from vital signs of the patient.Information technology is increasingly becoming widely used in growing businesses and improving productivity. We recommend that you consider purchasing documents that standardize their usage on a global scale. Check out the top cen catalog standards en-iso-8536-10-2004 review.



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قديم 11-19-2021, 05:27 PM   رقم المشاركة : [15]
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قديم 11-23-2021, 06:02 AM   رقم المشاركة : [16]
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قديم 11-30-2021, 07:02 AM   رقم المشاركة : [18]
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قديم 12-03-2021, 12:51 AM   رقم المشاركة : [19]
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قديم 12-03-2021, 12:59 AM   رقم المشاركة : [20]
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