10-13-2021, 12:48 PM
Medical Electrical Equipment - Part 2-3 Specific Requirements For The Basic Safety And Essential Effectiveness Of Equipment Used For Short-Wave Therapy En 60601-2-3:2015
Short-wave therapy is extensively used today in the medical field. That is why importance of regulation dramatically arose. IEC 60601-2-3.2012 describes the basic safety requirements and the essential performance of equipment used for therapeutic use in short waves. Short-wave treatment equipment is medical equipment that is designed to offer therapeutic treatment of patients through the use of magnetic or electric fields. They are not classified as equipment capable of producing electromagnetic fields at frequencies exceeding 13 MHz but not exceeding 45 MHz. Iteh can be reached for more details about this document, as it is of a very narrow area of coverage. Check out the most popular iso catalog standards iso-r-1938-1971 site.
Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
In our modern world, a creative management system is crucial for building a profitable business structure. It is therefore important to keep an eye on the regulatory documents that govern the system from its inception to its final stage. EN ISO 56002 will come into effect in 2021.This document provides guidance to help you establish an, establish, maintain and continuously enhance your innovation management process. It can be used by all existing organizations. It can be used for:a) Organizations that want to achieve sustained success , by demonstrating their capability and ability to handle innovative activities effectively in order to produce the outcomes they expect.B. Customers and customers who are interested in the organization's innovative capabilities.c. Organizations and interested individuals looking to improve communication through a shared understanding of the characteristics of an innovation management system.D. providers that provide courses in assessment, training or consultation for innovation management.E. policymakers, seeking to increase the efficiency and effectiveness of support programs that aim at enhancing the ability to innovate and improve the competitiveness of organizations and development in society.1.2 The guidelines contained in this document are general and is designed to be used in conjunction with:a) All kinds of organizations regardless of type, size, or sector. While the emphasis is on established businesses but we also recognize that temporary and permanent businesses can benefit from these guidelines in part or in their entirety.b. All kinds of innovations, e.g. process, product, service model, method, etc, ranging from incremental to radical;C) various types of strategies, e.g. c) all types of approaches, e.g., internal and external innovation, market- and technology-based innovation activities, as well as design-driven innovation.It does not define the specific actions of an organization but provides general guidance. It does not prescribe any requirements or specific tools or techniques for innovation.If you're not sure about certain modifications in this document, we suggest you speak with an expert to verify whether the international standard is suitable to be implemented within your company's current structure. Have a look at the top clc catalog standards en-60745-2-15-2006 blog.
Characterization Of Bulk Material - Determination Of A Size Weighted Fine Fraction, Crystalline Silica And Crystallized Silicon Content - Part I: General Information And The Choice Of Tests EN 17289-1:2020
Regulators face a number of challenges due to the varying nature of the manufacturing materials. International standards are being created to allow organizations and companies to expand their market.This document provides the necessary needs and possibilities for selecting the best test method to determine the size-weighted percentage of crystallized silica as well as the SWFFCS of bulk materials.This document gives guidelines on how you can prepare the sample, and then determine crystalline silica using X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 17289-2 refers to a method of formulating the size-weighted fine fraction based on a measured size distribution. This assumes that the distribution of silica crystals particles in bulk materials is similar. EN 17289-3 describes how to calculate the size-weighted fine percentage of crystalline silicona by using liquid sedimentation. Both methods are based on certain limitations and assumptions that are outlined in EN 17289-2 and EN 17289-3, respectively. If the method is validated and studied using the EN 17289-3 method can be used to calculate other constituents.This document is suitable for bulk silica-containing crystalline materials that have been thoroughly studied and verified for the analysis of the size-weighted fraction and crystalline silica.If your work area is in direct contact with one of the substances mentioned in this document, including it in your documentation base for technology will greatly aid the process of increasing production. Visit our website to learn more. Check out the best iso catalog standards iso-r-38-1957 review.
Safety Of Machine Tools Presses Part 4 Safety Requirements For Pneumatic Presses (Iso 160922-4.2019) EN ISO 16092-4:2020
Safety is always an essential aspect in establishing the regulatory framework that is applicable to an industry or organization. That's why there are numerous international standards that affect this issue. One of the most important is EN ISO 160922-4: 2020.This document, along with ISO 16092-1, outlines the technical safety requirements and the measures that must be followed by persons undertaking the design, manufacture and supply of pneumatic presses which are designed to process cold metal or material partly of cold metal.This document discusses all potential dangers for pneumatic presses. It is recommended that they be used according to their intended purpose and in conditions of misuse that are reasonably predictable by the maker. (See Clause 4). All of these phases are listed in ISO 12100 :2010, Section 5.4.You can clarify the technical specifications, and get in touch with us if you are looking to purchase the document. See the most popular cen catalog standards en-17106-1-2021 blog.
Health InformaticsInteroperability Between Devices. Part 20701 - Point-Of-Care-Based Medical Communication. Medical Devices That Are Service-Oriented Exchange Architecture And Binding To Protocols. (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
Not only are communication technologies employed in fields closely linked to this group however, they are also utilized in the medical sector. Because the introduction of multiple medical devices is complex and requires the restructuring of existing systems international documents are developed to assist in these processes.
This standard's scope is to define a service-oriented medical device architecture and communication protocol specification for distributed system of Point-of-Care (PoC) medical devices and medical IT systems that require to exchange data or regulate networks of PoC medical devices. It describes the functional elements and their communication relationships, as well as how they are linked to the protocol specifications.This document is highly specialized and has been narrowly focused. We recommend that you study its technical parameters and consult professionals who are knowledgeable about the international selection of documents. Check out the top cen catalog standards en-4705-2020 info.
![[Image: 1455128036810.png]](http://www.proftesting.com/blog/wp-content/uploads/2016/03/1455128036810.png)
Short-wave therapy is extensively used today in the medical field. That is why importance of regulation dramatically arose. IEC 60601-2-3.2012 describes the basic safety requirements and the essential performance of equipment used for therapeutic use in short waves. Short-wave treatment equipment is medical equipment that is designed to offer therapeutic treatment of patients through the use of magnetic or electric fields. They are not classified as equipment capable of producing electromagnetic fields at frequencies exceeding 13 MHz but not exceeding 45 MHz. Iteh can be reached for more details about this document, as it is of a very narrow area of coverage. Check out the most popular iso catalog standards iso-r-1938-1971 site.
Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
In our modern world, a creative management system is crucial for building a profitable business structure. It is therefore important to keep an eye on the regulatory documents that govern the system from its inception to its final stage. EN ISO 56002 will come into effect in 2021.This document provides guidance to help you establish an, establish, maintain and continuously enhance your innovation management process. It can be used by all existing organizations. It can be used for:a) Organizations that want to achieve sustained success , by demonstrating their capability and ability to handle innovative activities effectively in order to produce the outcomes they expect.B. Customers and customers who are interested in the organization's innovative capabilities.c. Organizations and interested individuals looking to improve communication through a shared understanding of the characteristics of an innovation management system.D. providers that provide courses in assessment, training or consultation for innovation management.E. policymakers, seeking to increase the efficiency and effectiveness of support programs that aim at enhancing the ability to innovate and improve the competitiveness of organizations and development in society.1.2 The guidelines contained in this document are general and is designed to be used in conjunction with:a) All kinds of organizations regardless of type, size, or sector. While the emphasis is on established businesses but we also recognize that temporary and permanent businesses can benefit from these guidelines in part or in their entirety.b. All kinds of innovations, e.g. process, product, service model, method, etc, ranging from incremental to radical;C) various types of strategies, e.g. c) all types of approaches, e.g., internal and external innovation, market- and technology-based innovation activities, as well as design-driven innovation.It does not define the specific actions of an organization but provides general guidance. It does not prescribe any requirements or specific tools or techniques for innovation.If you're not sure about certain modifications in this document, we suggest you speak with an expert to verify whether the international standard is suitable to be implemented within your company's current structure. Have a look at the top clc catalog standards en-60745-2-15-2006 blog.
Characterization Of Bulk Material - Determination Of A Size Weighted Fine Fraction, Crystalline Silica And Crystallized Silicon Content - Part I: General Information And The Choice Of Tests EN 17289-1:2020
Regulators face a number of challenges due to the varying nature of the manufacturing materials. International standards are being created to allow organizations and companies to expand their market.This document provides the necessary needs and possibilities for selecting the best test method to determine the size-weighted percentage of crystallized silica as well as the SWFFCS of bulk materials.This document gives guidelines on how you can prepare the sample, and then determine crystalline silica using X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 17289-2 refers to a method of formulating the size-weighted fine fraction based on a measured size distribution. This assumes that the distribution of silica crystals particles in bulk materials is similar. EN 17289-3 describes how to calculate the size-weighted fine percentage of crystalline silicona by using liquid sedimentation. Both methods are based on certain limitations and assumptions that are outlined in EN 17289-2 and EN 17289-3, respectively. If the method is validated and studied using the EN 17289-3 method can be used to calculate other constituents.This document is suitable for bulk silica-containing crystalline materials that have been thoroughly studied and verified for the analysis of the size-weighted fraction and crystalline silica.If your work area is in direct contact with one of the substances mentioned in this document, including it in your documentation base for technology will greatly aid the process of increasing production. Visit our website to learn more. Check out the best iso catalog standards iso-r-38-1957 review.
Safety Of Machine Tools Presses Part 4 Safety Requirements For Pneumatic Presses (Iso 160922-4.2019) EN ISO 16092-4:2020
Safety is always an essential aspect in establishing the regulatory framework that is applicable to an industry or organization. That's why there are numerous international standards that affect this issue. One of the most important is EN ISO 160922-4: 2020.This document, along with ISO 16092-1, outlines the technical safety requirements and the measures that must be followed by persons undertaking the design, manufacture and supply of pneumatic presses which are designed to process cold metal or material partly of cold metal.This document discusses all potential dangers for pneumatic presses. It is recommended that they be used according to their intended purpose and in conditions of misuse that are reasonably predictable by the maker. (See Clause 4). All of these phases are listed in ISO 12100 :2010, Section 5.4.You can clarify the technical specifications, and get in touch with us if you are looking to purchase the document. See the most popular cen catalog standards en-17106-1-2021 blog.
Health InformaticsInteroperability Between Devices. Part 20701 - Point-Of-Care-Based Medical Communication. Medical Devices That Are Service-Oriented Exchange Architecture And Binding To Protocols. (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
Not only are communication technologies employed in fields closely linked to this group however, they are also utilized in the medical sector. Because the introduction of multiple medical devices is complex and requires the restructuring of existing systems international documents are developed to assist in these processes.
This standard's scope is to define a service-oriented medical device architecture and communication protocol specification for distributed system of Point-of-Care (PoC) medical devices and medical IT systems that require to exchange data or regulate networks of PoC medical devices. It describes the functional elements and their communication relationships, as well as how they are linked to the protocol specifications.This document is highly specialized and has been narrowly focused. We recommend that you study its technical parameters and consult professionals who are knowledgeable about the international selection of documents. Check out the top cen catalog standards en-4705-2020 info.