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发表于 2021-8-30 01:28:38 | 显示全部楼层 |阅读模式
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发表于 2021-9-29 02:28:33 | 显示全部楼层

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发表于 2021-10-13 23:39:54 | 显示全部楼层

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

Part 1-11 Of The Medical Electrical Equipment - Collateral Standard: The Requirements For Medical Equipment And Medical Electronic Systems Utilized In The Home Healthcare Environment En 60601-1-11: 2015
Everyday, the need for home healthcare environments is increasing. The process of developing special standards for this field isn't over. The International Standard addresses the essential safety and performance of medical equipment and systems that are used in the home healthcare environment. The International Standard is applicable regardless of whether the equipment or system are designed to be utilized by non-trained or skilled healthcare personnel. It provides in depth the procedures to comply with all security demands. We are aware of the importance of standards consciousness even for medical equipment at home. Follow the link to keep informed of the latest information by following our website. Check out the most popular iec catalog standards iec-61937-1-2007amd1-2011-csv info.

Innovation Management - Tools And Techniques To Foster Innovation Partnerships Guideline (Iso 56003:2019) En Iso 56003:2021
The development of the best partnerships is key in the development and promotion of new products. This permits the exchange of ideas, suggestions in addition to financial and other support along with other aspects necessary for the development of an effective system. EN ISO 56003-2021 is an international standard that offers guidelines on how to build the most efficient partnerships.This document provides guidance on partnership in innovation. It offers guidelines for innovation partnerships.Choosing whether or not to join an Innovation PartnershipFind, evaluate, and select partnersIn sync with the perceptions of your partner of value, and their challenges.Manage interactions with partnersThe guidelines in this document are applicable to all types of collaboration or partnership and is intended to be applied to any organization, regardless of its size, size, type of product/service, and type.A) startups that collaborate with larger companies;b) SMEs or larger organizations;c) private sector entities with public or academic institutions;D. Public, academic and not-for-profit institutionsStart with a gap assessment first, then identify and engage potential innovation partners. And finally, manage their interaction.This standard is ideal for both start-ups and established companies. Collaboration is crucial and is often the primary to a successful development and scaling. We recommend this document to anyone who is seeking long-term growth. Have a look at the best cen catalog standards en-1335-1-2000-ac-2002 info.

Characterization Of Bulk Materials – The Determination Of A Weighted Size Fine Fraction Or Crystalline Silica Contents - Part I: Basic Information And Choice Of Test Method EN 17289-1:2020
The diversity of the products used complicates the regulation process both locally and globally. International standards are currently being developed to facilitate businesses and organizations who want to access new markets.This document specifies the specifications and test methods to determine the size of the size-weighted fine fraction (SWFF) and the size-weighted fine fraction of crystallized silica (SWFFCS) in bulk materials.This document provides guidelines on how to prepare the sample, and then determine crystallized silica using X-ray difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 17178-2 provides a method to calculate the size-weighted fraction of fine particles based on a measured size distribution. It is based on the assumption that the size distribution for crystal quartz particles are identical to that of other particles found in the bulk material. EN 1789-3 describes a procedure that employs a liquid sedimentation method to determine the size-weighted fine fraction of silica crystalline. Both methods are restricted in their scope and rely on certain assumptions. The EN 17289-3 method is also applicable to other constituents than CS when it is validated.This document may be used for bulk silica-containing crystalline materials, provided that it has been thoroughly studied and validated to allow for the evaluation of size-weighted fine particles and crystallized silica.If your business comes into contact with the material described in the description, then it can be a huge opportunity to increase production. The link to our site provides more detail. See the best cen catalog standards en-14211-2012 info.

Security Of Machine Tools - Pneumatic Presses – Part 4. (Iso 160922-4.2019). EN ISO 16092-4:2020
Safety concerns are an important aspect of creating an appropriate regulatory framework for any production or organization. This is the reason why there are a variety of international standards that cover the issue.This document, along with ISO 16092-1, defines the technical safety requirements and procedures to be implemented by anyone involved in the development, manufacturing and supply of pneumatic presses which are intended to work on cold metal or material made composed of cold metal.This document outlines all possible dangers that could be a concern for pneumatic presses. It is recommended to use them for the purpose they were designed and in conditions of misuse that are reasonably predictable by the maker. (See the Clause 4). Every phase of the machine's life-span as described in ISO 12100, 2010, 5.4 were taken into consideration.If you're interested in purchasing this document, please follow the link to view all the technical specifications. Contact the team who will explain all information. Have a look at the recommended sist catalog standards sist-en-1904-2002 site.

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
Medical device related documents may contain many different parts. They can complement one with respect to their respective functions, and can be discussing entirely different technologies. EN ISO 1073/10201 IEEE 2020.The goal of this project is to develop a general object-oriented model information which can be used to categorize information and determine the types of services utilized to facilitate point-of-care (POC) medical devices ' communications. The scope of this project is focused mainly on medical equipment for acute care and the vital sign for communication of patients information.Information technology is being used more and more to boost business efficiency and productivity. We suggest that you look into purchasing documents that will standardize their use globally. Have a look at the top rated cen catalog standards en-998-1-2016 info.

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