Part 2-11: Safety And Performance Requirements For Electrical Equipment Used In Medical Care En 60601-2-11:2015
Sometimes, medical equipment may be used for treatment but also causing some dangerous effects after. It is mandatory to use equipment during these situations to decrease the possibility of negative effects. EN 60601-2-11.2015 is a document which outlines this kind of scenario. This document covers the essential safety and performance of gamma-beam therapy equipment, and also multi-source stereotactic devices for radiotherapy. This particular standard of the 60601 series, establishes the requirements that must be adhered to by manufacturers in the development and construction of gamma beam therapy equipment. To prevent dangerous situations, the standard outlines tolerance levels for interlocks to be used to prevent interruption or termination of radiation. Each standard specifies the kind of tests that are done by the manufacturer and site tests. If your manufacturer is using the gamma therapy equipment that is in use, you can get familiar with our standards by going to the Item website. See the top
iso catalog standards iso-iec-ts-20071-15-2017 site.
Innovation Management - Fundamentals And Vocabulary (Iso 56000:2020). EN ISO 56000:2021
Documents that explain can be made for technical standards, such as providing information security. This is in order to avoid confusion about the meaning of the word. EN ISO 56000, 2021 is an example. This document outlines the fundamental concepts, terminology and the principles of innovation management, as well as their methodical implementation. It can be used for:A) Organisations who implement an innovation management strategy , or conduct assessments of innovation management.b) organizations that need to increase their capability to efficiently manage innovation;c. users, customers, and other relevant parties (e.g. suppliers, partners, funding organizations as well as universities, investors, and government officials) trying to establish confidence in the capabilities of innovation of an organization;d) companies and other parties seeking to improve communication through a common knowledge of the terms employed in innovation managementE) Training providers for, assessment or consulting regarding innovation management and its systems.F. Developers and users of standards related to innovation management.1.2 This document should be applicable to all types of organizations regardless of their size or maturity, sector, kind.b. All kinds of innovations, e.g. You can have a item, service, or model.C. All approaches (e.g. Open and internal innovation technological-based, market-based, and design-driven innovation activities.This document defines the terms employed in all ISO/TC279 standards related to innovation management.The standard is packed with important clarifications. We recommend that your go through them thoroughly and cross-check their accuracy with your technological base to make certain that they are the best document for you to use to promote your business internationally. Check out the most popular
cen catalog standards en-13189-2000-ac-2002 blog.
Bulk Materials For Characterization - Determination Of Size-Weighted Fine Fractions And The Content Of Crystalline Silica - Part 1 General Information And The Selection Of Testing Methods EN 17289-1:2020
Regulators face significant challenges because of the variability in the materials used in production. International standards are being established to make it easier for organisations and companies to gain access to new markets.This document details the requirements to determine the size weighted fine fraction (SWFF) and the size weighted fine fragment crystalline silica (SWFFCS).This document contains guidance regarding the preparation and measurement of crystallized Silica using Xray-ray Powder Diffractometry (XRD) or Fourier Transform Infrared Spectroscopy.EN 1789-2 describes the method of getting the size weighted fine fraction based on a measured distribution of particle sizes. This assumes that the distribution of silica crystals particles in bulk material is the same. EN 17289-3 describes a liquid sedimentation method for determining the size-weighted fine portion of crystalline silica. Both methods have limitations and assumptions. These limitations are outlined in EN 17289-2, EN 17289-3. If the method is validated correctly it is possible that the EN 17289-3 methodology can apply to different constituents.This document is applicable to the bulk materials containing crystalline silicona that have been thoroughly studied and validated in order to evaluate the size-weighted fine fraction, as well as crystallinesilica.The existence of the technology documentation base will help you scale up production when your industry is in direct contact with the information contained in this document. More information is available on our site. Have a look at the best
cen catalog standards en-2608-2005 info.
Software Engineering Systems - Software Product Quality Requirements Evaluations (Square). Common Industry Formats (Cif) To Ensure Usability. Specification For User Requirements (Iso 25065.2019). EN ISO 25065:2020
The main advantages of having a top spot in the global market is the quality of the software. To comprehend the regulations of these markets, it is essential to know the international standards that must be observed in the present. These requirements are contained in documents such as EN ISO 25065 2020.This document offers a common structure and language for defining the needs of the user. This document defines the industry standard (CIF) for user requirements specifications, which include the content elements, as well as the format to express them.A specification of user requirements is the formal description of a specific set of user specifications that assist in the creation of interactive systems.This document refers to the user's requirements. These include: a) requirements for interactions between the user and the system in order to attain the desired results (including specifications regarding outputs of the system and attributes); and b) quality requirements pertaining to interaction with the system. These quality requirements can be used as a basis to determine the approval of the system.ISO/IEC 25030 specifies quality requirements. This document includes a special type of quality obligation called usage-related requirements. The content elements in the user specification are intended to be used in documentation that results from activities listed in ISO9241-210 and human-centered design methods such ISO9241-220.This document is designed to be used as a guideline by business analysts, requirements engineers and product managers. It may also be used for product owners who are acquiring systems from third-party suppliers. CIF's standards cover usability-related information (as specified in ISO 9241-11 & ISO/IEC TR25060).The requirements of the user may not just be related to usability, but may can also encompass other perspectives such as human-centered quality, ISO 9241-220, ISO/IEC TS 25011 ISO/IEC 25030, and other quality perspectives within ISO/IEC 25010.The guidelines were originally created to be used in interactive systems. However, it is able to be used for all types of domains. The document does not prescribe any method, lifecycle or procedure. The content elements of specifications for user requirements can be utilized for iterative development, which involves the development and refinement of requirements (e.g. as in agile development).
Utilizing this international standard will greatly simplify your professional activities as well as help you structure the existing system, and create new opportunities for conquering new markets and scaling your company. Have a look at the most popular
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Health Informatics -- Standard Communication Protocol - Computer-Aided Electrocardiography EN 1064:2020
While it was only a decade ago that medical technology was being introduced to the world, the situation has changed over the last few years. With increased attention given to the human body, advancements and progress in the field of medicine are now being focused on in particular. This industry is responsible to protect the human body. Therefore, much attention is given to information security. It is regulated by international standards like EN 1064:2020.This document outlines the standard conventions for the cart to cart exchange and cart-to-cart swap of patient information. This document describes the structure and contents of the data that will be exchanged between digital ECG carts, computers ECG management system systems, and other systems on computers that store ECG data.This standard can give significant boost to your company's development in the modern market. We recommend to read the rules and click on the link to find out more. Check out the best
iec catalog standards iec-60423-2007 information.