10-13-2021, 04:45 PM
Medical Electrical Equipment - Part 1-9: General Requirements For Basic Safety And Performance Essential To A High Standard - Collateral Standard: Requirements For Environmentally Conscious Design En 60601-1-9:2008
The environment is at the heart of human existence. Technologies are constantly changing. It is vital to guarantee the safety of all new systems. That is the reason why new standards for medical equipment, which regulate the protection of the environment are being developed. This collateral standard aims to enhance the environmental quality of all medical electrical equipment. It is based on all aspects of the lifecycle of the product, including product specification and design, manufacturing logistics, sales installation, and usage. This means protecting the environment and human health from hazardous substances, conserving energy and raw materials, minimizing the generation of waste, as well as minimizing negative environmental impact of the disposal of waste. The criteria needed to reach this goal should be incorporated into every stage of the medical electrical equipment life cycle from the specification stage to final management of the life cycle. For more information, please go to the website. Check out the recommended iso catalog standards iso-iec-tr-24800-1-2012 site.
Innovation Management - Fundamentals And Vocabulary (Iso 56000 :2020). EN ISO 56000:2021
Explanatory documents may be required to comply with certain standards of technology. For instance, they could be required to provide a rationale for information security. EN ISO 56000: 2021, is a good example. This document contains the essential terms and concepts for managing innovation as well as its systematic implementation. It can be used for:A) Organizations which have implemented an innovation management system;B. Organizations that need help in managing innovation activitiesc) Customers, users, and other interested parties (e.g. suppliers, partners, funders, investors, universities and government officials) trying to establish confidence in the capabilities of innovation of the organization;d) organisations and other interested individuals who wish to improve communication via a shared understanding of the vocabulary that is used in innovation management(e) Providers for training in, assessment or consulting regarding innovation management and its systems.F) the creators of innovation management and related standards.1.2 This document is applicable to:b) all types of innovations, e.g. Model, product, service and method could all be considered starting from incremental and ending with the radical.c. Any kind of approach that include. Internal and open innovation driven by technology and markets innovations.This document defines the terms and definitions applicable to all innovation management and management system standards developed by ISO/TC 279.These features of clarification are numerous and we suggest that each feature be thoroughly scrutinized and compared with the technological foundation of your company. This will help you promote your organization effectively at international levels. Have a look at the recommended sist catalog standards sist-en-301-455-2-v1.3.1-2005 information.
The Characterisation Of Bulk Materials - Determination A Size-Weighted Fine Fraction And Crystalline Silica Content - Part 2 Method Of Calculation EN 17289-2:2020
Many parts could be combined into one standard that covers a variety of areas. EN 17289-2 is the 2020 version.This document explains how you can calculate the size-weighted fine portion (SWFF) and size-weighted small portion of crystallized silicona (SWFFCS). The document also defines the assumptions and prerequisites that must be met in order for this method to be considered valid.This document contains details to help users assess bulk materials in terms of their size-weighted crystalline size and fine fraction.Annexe A offers a specific procedure to determine the SWFF of diatomaceous earth bulk materials. The internal porosity and the effective density of diatomaceous soil requires that the general instructions in this document are modified.This document applies to the bulk materials containing crystalline silicona that have been thoroughly studied and validated to determine the size-weighted fine fraction as well as crystallinesilica.For a clearer understanding of the need for the standards in question, it's essential to examine the technical parameters used in production standards with the requirements of the individual standards. If you have questions about the process, you can always contact the experts in international standards. Check out the top cen catalog standards en-1993-1-12-2007-ac-2009 site.
Methodology For Reducing The Environmental Impacts Of Product Design Production, Development, And Development EN 16524:2020
Environmental and safety issues evolve as new technologies and air pollution emerge. EN 16524 2020 is a document that could help with this problem.This document describes a methodology for reducing the overall environmental impact of products through design and development that is tailored to mechanical items as specified in 3.1.This strategy is especially beneficial in the process of redesigning existing products. It can be employed to develop new products when you make the right assumptions regarding the (virtual reference) product. This approach is aimed at companies that have decided to integrate an ecodesign approach to optimise environmental impacts within the duration of the lifecycle of the product in conjunction with other product aspects, including functionality, quality, costs, etc.It also helps to meet certain specifications of ISO 14001:2015, which focuses on the integration of environmental aspects in the design of products. This document is aimed at those who are directly involved in the development and design of mechanical products, as well as executives who define corporate policies, and decision-makers. The method proposed is designed to encourage ecodesign efforts within companies.The document also includes an example template that companies can use for communicating their environmental approach. The document was not intended to permit you to compare the products of various suppliers. This document cannot be used for product certification.This document is relevant especially in the 21st century. This is why you need to be aware of the possibility of getting the document and incorporating it into the operations of your organization. Check out the best iso catalog standards iso-ts-12869-2012 blog.
Health Informatics - Device Interoperability Part . 20701 Point-Of-Care Communications With Medical Devices - Medical Device Exchange With A Service-Oriented Architecture (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
These technologies are not only utilized in the areas which fall under the umbrella of this classification, but also in the medical sector. The development of medical devices require a intricate transformation. To make these processes easier, international documents have been made.
This standard covers a service-oriented design for medical devices, and communication protocol specifications for medical IT systems. These systems for medical IT must be able to safely and securely control PoC medical devices. It defines functional components, their communication relations and the connecting of these components and their communication relations to protocol specifications.This document is specialized and has been narrowly focused. We suggest that you study its technical parameters and consult the managers who are experts in international document choice. Check out the top sist catalog standards sist-en-60193-2001 site.
![[Изображение: 1455128036810.png]](http://www.proftesting.com/blog/wp-content/uploads/2016/03/1455128036810.png)
The environment is at the heart of human existence. Technologies are constantly changing. It is vital to guarantee the safety of all new systems. That is the reason why new standards for medical equipment, which regulate the protection of the environment are being developed. This collateral standard aims to enhance the environmental quality of all medical electrical equipment. It is based on all aspects of the lifecycle of the product, including product specification and design, manufacturing logistics, sales installation, and usage. This means protecting the environment and human health from hazardous substances, conserving energy and raw materials, minimizing the generation of waste, as well as minimizing negative environmental impact of the disposal of waste. The criteria needed to reach this goal should be incorporated into every stage of the medical electrical equipment life cycle from the specification stage to final management of the life cycle. For more information, please go to the website. Check out the recommended iso catalog standards iso-iec-tr-24800-1-2012 site.
Innovation Management - Fundamentals And Vocabulary (Iso 56000 :2020). EN ISO 56000:2021
Explanatory documents may be required to comply with certain standards of technology. For instance, they could be required to provide a rationale for information security. EN ISO 56000: 2021, is a good example. This document contains the essential terms and concepts for managing innovation as well as its systematic implementation. It can be used for:A) Organizations which have implemented an innovation management system;B. Organizations that need help in managing innovation activitiesc) Customers, users, and other interested parties (e.g. suppliers, partners, funders, investors, universities and government officials) trying to establish confidence in the capabilities of innovation of the organization;d) organisations and other interested individuals who wish to improve communication via a shared understanding of the vocabulary that is used in innovation management(e) Providers for training in, assessment or consulting regarding innovation management and its systems.F) the creators of innovation management and related standards.1.2 This document is applicable to:b) all types of innovations, e.g. Model, product, service and method could all be considered starting from incremental and ending with the radical.c. Any kind of approach that include. Internal and open innovation driven by technology and markets innovations.This document defines the terms and definitions applicable to all innovation management and management system standards developed by ISO/TC 279.These features of clarification are numerous and we suggest that each feature be thoroughly scrutinized and compared with the technological foundation of your company. This will help you promote your organization effectively at international levels. Have a look at the recommended sist catalog standards sist-en-301-455-2-v1.3.1-2005 information.
The Characterisation Of Bulk Materials - Determination A Size-Weighted Fine Fraction And Crystalline Silica Content - Part 2 Method Of Calculation EN 17289-2:2020
Many parts could be combined into one standard that covers a variety of areas. EN 17289-2 is the 2020 version.This document explains how you can calculate the size-weighted fine portion (SWFF) and size-weighted small portion of crystallized silicona (SWFFCS). The document also defines the assumptions and prerequisites that must be met in order for this method to be considered valid.This document contains details to help users assess bulk materials in terms of their size-weighted crystalline size and fine fraction.Annexe A offers a specific procedure to determine the SWFF of diatomaceous earth bulk materials. The internal porosity and the effective density of diatomaceous soil requires that the general instructions in this document are modified.This document applies to the bulk materials containing crystalline silicona that have been thoroughly studied and validated to determine the size-weighted fine fraction as well as crystallinesilica.For a clearer understanding of the need for the standards in question, it's essential to examine the technical parameters used in production standards with the requirements of the individual standards. If you have questions about the process, you can always contact the experts in international standards. Check out the top cen catalog standards en-1993-1-12-2007-ac-2009 site.
Methodology For Reducing The Environmental Impacts Of Product Design Production, Development, And Development EN 16524:2020
Environmental and safety issues evolve as new technologies and air pollution emerge. EN 16524 2020 is a document that could help with this problem.This document describes a methodology for reducing the overall environmental impact of products through design and development that is tailored to mechanical items as specified in 3.1.This strategy is especially beneficial in the process of redesigning existing products. It can be employed to develop new products when you make the right assumptions regarding the (virtual reference) product. This approach is aimed at companies that have decided to integrate an ecodesign approach to optimise environmental impacts within the duration of the lifecycle of the product in conjunction with other product aspects, including functionality, quality, costs, etc.It also helps to meet certain specifications of ISO 14001:2015, which focuses on the integration of environmental aspects in the design of products. This document is aimed at those who are directly involved in the development and design of mechanical products, as well as executives who define corporate policies, and decision-makers. The method proposed is designed to encourage ecodesign efforts within companies.The document also includes an example template that companies can use for communicating their environmental approach. The document was not intended to permit you to compare the products of various suppliers. This document cannot be used for product certification.This document is relevant especially in the 21st century. This is why you need to be aware of the possibility of getting the document and incorporating it into the operations of your organization. Check out the best iso catalog standards iso-ts-12869-2012 blog.
Health Informatics - Device Interoperability Part . 20701 Point-Of-Care Communications With Medical Devices - Medical Device Exchange With A Service-Oriented Architecture (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
These technologies are not only utilized in the areas which fall under the umbrella of this classification, but also in the medical sector. The development of medical devices require a intricate transformation. To make these processes easier, international documents have been made.
This standard covers a service-oriented design for medical devices, and communication protocol specifications for medical IT systems. These systems for medical IT must be able to safely and securely control PoC medical devices. It defines functional components, their communication relations and the connecting of these components and their communication relations to protocol specifications.This document is specialized and has been narrowly focused. We suggest that you study its technical parameters and consult the managers who are experts in international document choice. Check out the top sist catalog standards sist-en-60193-2001 site.