10-13-2021, 02:47 PM
Medical Electrical Equipment - Part 2 Specific Requirements For Fundamental Safety And Performance Of Equipment For Short-Wave Therapy En 60601-2-3:2015
Short-wave therapy is extensively used today in the medical field. This is the reason why regulation of short-wave therapy is crucial. IEC 60601-2-3.2012 sets out the safety requirements and vital performance of short wave therapy equipment. Medical equipment that uses short-wave radiation therapy to treat patients is defined as equipment that exposes them to electric or magnetic fields that have frequencies higher than 13MHz, but lower than 45MHz. Iteh is suggested to go through this document as it has a limited specification. Check out the most popular iso catalog standards iso-iec-ieee-15939-2017 site.
Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Nowadays, a modern management system is vital for creating a successful company. This is why it's important that you be aware of the rules that govern it. EN ISO 56002: 2021 is one of them.This document offers guidance on how to set up, implement, maintain and enhance the effectiveness of an innovation management program that is applicable throughout all businesses. This document is applicable to:A) companies that strive to achieve sustained success by proving their ability to manage effectively innovations to get the results they want.b) customers, users and other interested parties, seeking confidence in the innovation capabilities of an organization.c) organizations and interested parties who seek to improve communication by a common understanding about what is an innovative management system.D. Providers of training in or assessment of innovation management or consulting to support it;E. Policy makers, who seek to improve their effectiveness in support programs targeted at innovation capabilities and competitiveness organizations and the development community.1.2 This document's guidance is general in nature and can be used by anyone who wishes to.A. All kinds of organizations regardless of size, sector, type or. The focus is on established companies however, it should be noted that both temporary and new businesses can also benefit from applying these guidelines to all or in part;B. All kinds and types of innovation, e.g. The product, service or process could be described as model or process, product or method. These innovations can vary from small to major.C) any of the methods, e.g. open and internal innovation market-, usertechnology and design-driven innovation activities.The document does not provide specific activities in an organization but rather provides guidelines on a general level. It doesn't prescribe any requirements or specific tools or techniques for innovation.We recommend speaking with a specialist if you are unsure about the suitability of certain modifications to this document for your organization. Have a look at the top rated cen catalog standards cen-ts-15531-5-2016 blog.
Bulk Materials For Characterization - Determination Of Size-Weighted Fine Particles And Crystalline Silica Content Part 1: General Information And Choice Of Testing Methods EN 17289-1:2020
The vast array of products and materials complicates regulation both locally, and globally. International standards are being created to facilitate the entry of businesses and organizations into new markets.This document defines the specifications and test methods to determine the size of the size-weighted fine fraction (SWFF) as well as the size-weighted fine fraction (SWFFCS) of crystalline silica (SWFFCS) in bulk materials.This document provides guidelines on how to prepare the sample and determine crystalline silica using X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 1789-2 describes a procedure to calculate the size-weighted fine fraction by measuring the size of particles distribution. However, it assumes, that the particle size distributions of the crystal particles are the same as those found in bulk material. EN 1789-3 provides the procedure for liquid sedimentation to determine the size weighted fine fraction of crystal silica. Both methods have their limitations and assumptions that are detailed in EN 17289-2 as well as EN 17289-3. If validated properly and validated, the EN 17289-3 method may also apply to different constituents.This document is applicable to crystallized silica with bulk material which has been thoroughly studied and validated for the assessment of the size-weighted, fine fraction and the crystallized silica.If your work area is in close contact with any of the items listed in this document, including it in your technological documentation base can greatly assist in the process of expanding production. Check out our website to find out more. Check out the recommended clc catalog tc clc-btwg-61-2 info.
Machine Tools Safety Presses - Part 4: Safety Specifications For Pneumatic Presses (Iso 16092-4:2019) EN ISO 16092-4:2020
Safety issues are always first considerations when creating a regulatory structure for a production business, which is the reason there are many of international standards that deal with the issue, one of the most notable is EN ISO 16092-4: 2020.This document, along with ISO 16092-2, provides technical safety requirements which must be adhered to by everyone who is responsible for the development, production and delivery of pneumatic presses designed to use cold metals or materials made up from cold steel.This document outlines all risks that could affect pneumatic presses when employed in line with their intended use and in conditions which are reasonably predicted by the maker (see Clause 4.) All phases, as per ISO 12100:2010, 5.4, have been taken into account.If you're interested in purchasing this document, you can follow the link to obtain all the technical information. You can also contact the team for clarification of any doubts. Have a look at the top rated iso catalog standards iso-19026-2015 blog.
Health Informatics – Device Interoperability Part 20701 Communication At The Point Of Care With Medical Devices . Service-Oriented Medical Device Exchange Architecture (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
This category includes areas like medicine, and communication technologies are used in these fields. The development of medical devices requires complex transformation. To ease these processes, international documents have been developed.
This standard defines a service-oriented design for medical devices, and protocols for communication in medical IT systems. Medical IT systems need to be able to secure and safely manage PoC medical gadgets. It identifies functional components, their communication relations and binding of components and communications relationships to protocol specifications.This document has a narrow outline and is extremely specific. Therefore, it is recommended that you review the technical specifications more carefully and when in doubt you seek out people who have experience choosing international documents. See the top rated sist catalog standards sist-iso-3972-2013-ac-2013 information.
![[图: management-system-organization-area-labe...012015.jpg]](https://png1.12png.com/14/16/16/1fdpAn2dCz/management-system-organization-area-label-iso-90012015.jpg)
Short-wave therapy is extensively used today in the medical field. This is the reason why regulation of short-wave therapy is crucial. IEC 60601-2-3.2012 sets out the safety requirements and vital performance of short wave therapy equipment. Medical equipment that uses short-wave radiation therapy to treat patients is defined as equipment that exposes them to electric or magnetic fields that have frequencies higher than 13MHz, but lower than 45MHz. Iteh is suggested to go through this document as it has a limited specification. Check out the most popular iso catalog standards iso-iec-ieee-15939-2017 site.
Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Nowadays, a modern management system is vital for creating a successful company. This is why it's important that you be aware of the rules that govern it. EN ISO 56002: 2021 is one of them.This document offers guidance on how to set up, implement, maintain and enhance the effectiveness of an innovation management program that is applicable throughout all businesses. This document is applicable to:A) companies that strive to achieve sustained success by proving their ability to manage effectively innovations to get the results they want.b) customers, users and other interested parties, seeking confidence in the innovation capabilities of an organization.c) organizations and interested parties who seek to improve communication by a common understanding about what is an innovative management system.D. Providers of training in or assessment of innovation management or consulting to support it;E. Policy makers, who seek to improve their effectiveness in support programs targeted at innovation capabilities and competitiveness organizations and the development community.1.2 This document's guidance is general in nature and can be used by anyone who wishes to.A. All kinds of organizations regardless of size, sector, type or. The focus is on established companies however, it should be noted that both temporary and new businesses can also benefit from applying these guidelines to all or in part;B. All kinds and types of innovation, e.g. The product, service or process could be described as model or process, product or method. These innovations can vary from small to major.C) any of the methods, e.g. open and internal innovation market-, usertechnology and design-driven innovation activities.The document does not provide specific activities in an organization but rather provides guidelines on a general level. It doesn't prescribe any requirements or specific tools or techniques for innovation.We recommend speaking with a specialist if you are unsure about the suitability of certain modifications to this document for your organization. Have a look at the top rated cen catalog standards cen-ts-15531-5-2016 blog.
Bulk Materials For Characterization - Determination Of Size-Weighted Fine Particles And Crystalline Silica Content Part 1: General Information And Choice Of Testing Methods EN 17289-1:2020
The vast array of products and materials complicates regulation both locally, and globally. International standards are being created to facilitate the entry of businesses and organizations into new markets.This document defines the specifications and test methods to determine the size of the size-weighted fine fraction (SWFF) as well as the size-weighted fine fraction (SWFFCS) of crystalline silica (SWFFCS) in bulk materials.This document provides guidelines on how to prepare the sample and determine crystalline silica using X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 1789-2 describes a procedure to calculate the size-weighted fine fraction by measuring the size of particles distribution. However, it assumes, that the particle size distributions of the crystal particles are the same as those found in bulk material. EN 1789-3 provides the procedure for liquid sedimentation to determine the size weighted fine fraction of crystal silica. Both methods have their limitations and assumptions that are detailed in EN 17289-2 as well as EN 17289-3. If validated properly and validated, the EN 17289-3 method may also apply to different constituents.This document is applicable to crystallized silica with bulk material which has been thoroughly studied and validated for the assessment of the size-weighted, fine fraction and the crystallized silica.If your work area is in close contact with any of the items listed in this document, including it in your technological documentation base can greatly assist in the process of expanding production. Check out our website to find out more. Check out the recommended clc catalog tc clc-btwg-61-2 info.
Machine Tools Safety Presses - Part 4: Safety Specifications For Pneumatic Presses (Iso 16092-4:2019) EN ISO 16092-4:2020
Safety issues are always first considerations when creating a regulatory structure for a production business, which is the reason there are many of international standards that deal with the issue, one of the most notable is EN ISO 16092-4: 2020.This document, along with ISO 16092-2, provides technical safety requirements which must be adhered to by everyone who is responsible for the development, production and delivery of pneumatic presses designed to use cold metals or materials made up from cold steel.This document outlines all risks that could affect pneumatic presses when employed in line with their intended use and in conditions which are reasonably predicted by the maker (see Clause 4.) All phases, as per ISO 12100:2010, 5.4, have been taken into account.If you're interested in purchasing this document, you can follow the link to obtain all the technical information. You can also contact the team for clarification of any doubts. Have a look at the top rated iso catalog standards iso-19026-2015 blog.
Health Informatics – Device Interoperability Part 20701 Communication At The Point Of Care With Medical Devices . Service-Oriented Medical Device Exchange Architecture (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
This category includes areas like medicine, and communication technologies are used in these fields. The development of medical devices requires complex transformation. To ease these processes, international documents have been developed.
This standard defines a service-oriented design for medical devices, and protocols for communication in medical IT systems. Medical IT systems need to be able to secure and safely manage PoC medical gadgets. It identifies functional components, their communication relations and binding of components and communications relationships to protocol specifications.This document has a narrow outline and is extremely specific. Therefore, it is recommended that you review the technical specifications more carefully and when in doubt you seek out people who have experience choosing international documents. See the top rated sist catalog standards sist-iso-3972-2013-ac-2013 information.