Medical Electrical Equipment - Part 2-11: Particular Needs For The Safety Of The Fundamental And Vital Performance Of Gamma Beam Therapy Equipment En 60601-2-11:2015
Sometimes, medical equipment could be used as a treatment option but can also be dangerous. To reduce the risk of negative outcomes, equipment should be used in such cases. EN 60601-2-11.2015 can be a good example of this scenario. This document covers the basic safety and essential performances of gamma therapy equipment. The 60601 standard in question is part of that series. It specifies the rules that manufacturers should follow when developing and fabricating gamma beamed therapy equipment. It specifies tolerance limits that interlocks should not exceed in order to prevent, interrupt and terminate irradiation. For every requirement, there are specific requirements for type tests and site tests. Our standard is available to manufacturers who have the gamma radiation therapy equipment. Check out the top
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International Standardizations: Innovative Technologies
New technologies are taking over of the world. Every day each minute, every second, a new technology is developed, a different way of using existing technologies, and the world is inevitably changing in connection with this. Because of the significant influence of electronic machines as well as artificial intelligence on our lives as well as the fact that keeping them in chaos could have devastating effects for humanity. Also, keep in mind that the Internet and speedy data transfer increase the risk of data leakage, and security is becoming more crucial every day. Today, we'll provide technical guidance on where and how to utilize these techniques and the international standards that are responsible for data security. See the recommended
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Characterization Of Bulk Material - Determination A Size-Weighted Fine Fraction, Crystalline Silica And The Content Of Crystalline Silicon - Part I General Information And The Choice Of Tests EN 17289-1:2020
Regulators face significant challenges due to the variability in the materials used in production. International standards are being created to make it easier for firms and organisations into new markets.This document provides the specifications and choices of testing methods for the determination of the fine fraction of crystalline silicona (SWFFCS) as well as the size-weighted small fraction (SWFF).This document also provides guidance on how to prepare the sample, and the identification of crystallized silicona using Xray Powder Diffractometry XRD (XRD) and Fourier Transform Infrared Spectroscopy FT-IR (FT-IR).EN 17289-2 specifies a method to calculate the size-weighted fine fraction by measuring the size distribution. It also assumes that the particle size distribution of the crystalline silica particles is similar to the other particles found in the bulk material. EN 1789-3 provides a liquid sedimentation procedure to determine the size weighted fine silica fraction of crystal. The two methods are based upon a number of limitations and assumptions, which are outlined in EN 17289-2 and EN 1789-3, respectively. If the method is validated correctly and validated, the EN 17289-3 method can also apply to different constituents.This document can be used to evaluate bulk crystalline silica material, provided it has been thoroughly studied and verified to permit the assessment of size-weighted, fine particles and crystalline silica.The existence of the technology documentation base will help you scale up production if your area of activity is directly connected to the information contained in this document. For more detailed information you can refer to our site. See the recommended
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Safety Of Machine Tools - Presses - Part 4: Safety Requirements For Pneumatic Presses (Iso 16092-4:2019) EN ISO 16092-4:2020
Safety concerns are an important part of creating a regulatory framework for any production or organization. This is the reason the reason why there are a variety of international standards that deal with this issue.This document, in conjunction with ISO 16092-1, describes the technical safety requirements for persons involved in the development, production and distribution of pneumatic presses that are designed to work either of cold metal, or at least a part of cold metal.This document outlines all risks that could affect pneumatic presses if they are utilized in accordance to their intended purpose and under conditions of misuse that are reasonably predicted by the manufacturer (see Clause 4.) All of these phases are defined in ISO 12100 :2010, Section 5.4.If you are interested, click the link on our website to view the full technical specifications. Also, contact the team for any clarifications. Have a look at the best
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Health Informatics - Requirements For International Machine-Readable Codes For Medicinal Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As more and more technology becomes available, regulations are being created to regulate their use and limit the risk. EN ISO/ IEEE 11073-10201 is set for 2020. This document can be modified in the event of technological advances.This document offers instructions on the labelling and identification of medical products starting from the manufacturing of the medicinal product up until the point where the product is dispensable. This document outlines best practices for AIDC barcoding solutions. However, users should consider the coding interoperability requirements for other AIDC technologies, e.g. Radio Frequency IdentificationIf you have already used the previous version and wish to continue operating in the same activity field we suggest that you update this document with international rules and recommendations. Check out the best
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