Part 2-11: Specific Guidelines For The Security And Performance Of Equipment For Gamma-Beam Therapy En 60601-2-11:2015
Sometimes, medical equipment could be utilized to treat an illness, however, it can also trigger harmful side consequences. To minimize the chance of adverse effects medical equipment must be used. EN 60601-2-11.2015 is an example of such a scenario. This document addresses essential requirements for safety and performance for Gamma beam treatment equipment that includes stereotactic multi-source radiation therapy equipment. This particular standard of the 60601 series, lays out standards to be followed by the manufacturers when designing and manufacturing of gamma beam therapy equipment. It sets out tolerance limits that interlocks should not exceed to avoid interruption and termination of irradiation. Each requirement specifies the type tests performed by the manufacturer as well as site tests. Our standard is available to manufacturers who have Gamma radiation therapy equipment. Have a look at the recommended
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Information Technology Security TechniquesCode Of Practice For Information Security Controls Based On Iso/Iec 27002 For Cloud Services Iso/Iec 27017:2015
Information security concerns are being more and more prominent in the modern world. They affect every aspect of everyday life and also the overall structure of a company. ISO/IEC 270717 is an international standard that regulates the subject.ISO/IEC 27017:2015 gives guidelines for security measures for information applicable to the provision and use of cloud-based services. The guidelines include an additional guidance for implementation for the relevant controls defined in ISO/IEC 27002; - additional controls that include implementation guidance that specifically relate to cloud-based services. This Recommendation International Standard provides guidelines for implementation and controls for cloud service providers as well as cloud service customers.Given the many methods available for transferring information quickly today, we recommend that each method be explained in detail. Click here and go through all the technical specifications. Have a look at the most popular
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Characterization Of Bulk Materials – Determination Of A Size Weighted Fine Percentage Or Crystalline Silica Content - Part 2: Calculation Method EN 17289-2:2020
Many parts could be combined into a single standard that covers completely different areas. EN 17289-2 is the 2020 part.This document explains how to calculate the size-weighted crystalline silica fine fraction (SWFFF) and the size-weighted fine fraction (SWFFCS) for bulk materials. This document also provides assumptions and conditions that must be met in order to ensure this method to be valid.The aim of this document is to permit users to assess bulk materials based on their size weighted fine fraction and crystalline silica content.Annexe A contains an exact method to evaluate the SWFFs of bulk materials diatomaceous. Because of the diatomaceous's internal porosity earth, the general instructions provided in this document have been adapted in order to account for the material's effective density.This document can be used to evaluate crystal silica that contains bulk substances that have been thoroughly researched and verified for the evaluation of the fine fraction weighing size or crystal silica.It is possible to get a better idea of the importance of these standards through comparing the technical parameters of production standards with those of the individual standards. It is possible to seek the help of experts in the field of international standards if you have questions regarding the implementation of this stage. See the recommended
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Methodology To Minimize Environmental Impacts In The Development Of Products And In The Design Of Mechanical Products EN 16524:2020
As new methods of technology and air polluting emerge as new technologies and air pollutions become more prevalent, environmental and safety concerns are constantly evolving. EN 16524: 2020 is one of the documents that provides an answer.This document outlines a method to reducing the environmental footprint of production and design. This is applicable to mechanical products only, as described in 3.1.This method is ideal for designing a new product. If the assumptions concerning the virtual product are proven, the approach is also able to be used to create an entirely new product. The approach is targeted at businesses that are deciding to implement an ecodesign method to improve environmental impacts within the life-cycle of the product, with respect to other factors of the product such as functionality, quality, costs, etc.It meets a few of the specifications of ISO 14001 :2015 regarding the inclusion of environmental considerations in the design of products. This document is aimed at those directly involved in the design and developing mechanical products as well as decision-makers and managers who must establish corporate policies. The approach is intended as part to incite ecodesign efforts within companies.This document also contains an example template that companies can use to communicate their environmental approach. This document is neither intended nor suitable to compare products (even similar) of different suppliers. The document isn't suitable for certification of products.This document is extremely relevant for the 21st century. Therefore, you should be interested in acquiring it and incorporating it into your organization's activities. Check out the best
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Health Informatics Interoperability Of Devices. Part. 0701; Point-Of-Care Medical Device Communication. Architecture For Exchange Of Medical Instruments That Is Service-Oriented. Protocol Binding (Iso/Ieee 11073–20701 2020). EN ISO 11073-20701:2020
This covers areas such as medicine and communication technologies are employed in these fields. As the introduction of multiple medical devices is often complex and requires the restructuring existing systems, international documents are developed to assist in these processes.
This standard is a service-oriented Medical Device Architecture and Communication Protocol Specification distributed System of Point-of-Care(PoC) and medical devices, and medical IT Systems that require to exchange data and control PoC networked medical devices. It identifies functional components, their communication relations and the connecting of these components and their communications relations to protocols specifications.The document is specific and limited in the scope. As such, we recommend that you be reviewed for more information. If you have any questions, you can consult with managers who are specialists in international document selection. Check out the most popular
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