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Старый 15.09.2021, 21:02   #1
Silin Vladislav
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Старый 15.09.2021, 22:03   #2
Pisos
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Старый 21.09.2021, 01:21   #3
FrankJScott
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Старый 28.09.2021, 19:25   #4
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Старый 13.10.2021, 20:06   #5
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Part 1-9 Performance And Safety Requirements For Electrical Equipment Used In Medical Care. Collateral Standard: Design Aspects En 60601-1-9:2008
Environment is the name given to the lives of all people on Earth. As technology continues to evolve one of the most important things to do is to ensure that any new system is safe. The new standards for the environmental safety of medical equipment were created to address this issue. This standard is designed to improve the environment for all medical electrical equipment. It considers every aspect of the product's lifecycle which includes product specifications, design, manufacturing logistics, sales installation, and usage. This means protecting the environment and the people's health from toxic substances, while conserving the use of energy and raw materials, minimising the production of waste and reducing the negative environmental impacts that come with it. The criteria required to achieve this goal should be incorporated into every stage of the medical electrical equipment life-cycle, from the stage of specification through to end of life management. Find out more information on this document by going to the website. See the most popular iso catalog standards iso-asme-14414-2019 information.

Information Technology Security Techniques- Code For The Practice Of Information Security Controls In Accordance With Iso/Iec 27002 Cloud Services Iso/Iec 27017:2015
Security issues relating to information are more and more prominent in the modern world. They affect all aspects of daily life as well as the organisational structure of an organisation. One of the international standards for regulating this issue is ISO/IEC 2717:2015.ISO/IEC 270717:2015 provides guidelines for security measures which can be used for cloud provisioning and cloud services. It contains an additional set of guidelines for implementation in relation to ISO/IEC 27002 controls; - additional controls that have specific guidance for implementation. This Recommendation International Standard includes guidelines for implementation and controls for cloud service providers as well as cloud service users.There are many options for quick information transmission in the present. We recommend you review the links to this site to review all the technical parameters. Have a look at the top 53.020.99 catalog ics review.

The Characterisation Of Bulk Materials - Determination An Amount-Weighted Fine Fraction, And Crystalline Silica Content - Part 1: General Information And Choice Of Test Methods EN 17289-1:2020
The diversity of the materials used in production significantly hinders the regulatory process locally as well as globally. International standards are being developed to make it easier for businesses and organizations into new markets.This document describes the specifications and alternatives for choosing the most appropriate method of testing to determine the weighted size of crystallized silica and the SWFFCS of bulk materials.This document offers guidelines on how to prepare the sample, and then determine the crystalline silica by X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 17289-2 outlines a method for calculating size-weighted fine percentage using a measured particle size distribution. However, it assumes that the sizes of the crystalline particles are the same as the bulk material. EN 1789-3 provides the procedure for liquid sedimentation to calculate the size weighted fine fraction of crystal silica. Both methods are governed by the assumptions and limitations. The EN 17289-3 method is also suitable for other constituents than CS in the event that it is confirmed.This document is suitable to bulk crystalline silica materials that have been thoroughly examined and verified for analysis of the size-weighted fraction and the crystalline silica.If your field of work comes into direct contact with one of the items listed in this document, including it in your technical documentation base will greatly facilitate the process of expanding production. Find more details on our website. See the recommended iso catalog standards iso-iec-8613-10-1991-amd-5-1993 info.

Methodology To Reduce Environmental Impacts In The Development Of Products And In The Design Of Mechanical Products EN 16524:2020
As new technology and air pollution increase as do safety and environmental issues. EN 16524: 2020 is a document that could aid in solving this issue.This document outlines a strategy to reduce environmental impact through product development and design. It is specific to mechanical products as described in 3.1.This method is best for redesigning an existing product; it could also be used for the design of an entirely new product, provided that the appropriate assumptions about the (virtual) reference product are taken. This approach is employed by businesses that have adopted an ecodesign approach to minimise environmental impact throughout the life of their product.It helps meet certain requirements in ISO 14001, 2015 on the integration of environmental issues into the design of products. This document is intended for those who directly participate in the design and production of mechanical goods. The proposed method is designed to assist companies in launching ecodesign projects as part of an ongoing improvement and education approach.There is also a template in this document that companies could use to present their environmental policies. This document is neither intended or suitable for comparing the products (even similar) of different suppliers. This document is not designed nor suitable for product certification purposes.This document is particularly relevant for the 21st century and you must think about the possibility of purchasing the document and integrate it into the business activities of your organization. See the recommended iso catalog standards iso-16632-2021 information.

Health Informatics - Requirements For International Machine Readable Coding Of Medicinal Package Identifiers ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies are developed and improved, there will be more regulations to govern their use, and limit risks. EN ISO11073/10201 is 2020. This document is able to be modified in the event of technological advances.This document provides guidelines on the identification and labelling of medicinal products, starting from the point of manufacture of packaged medicinal product to the point at which you can dispensing the medicine. This document outlines best practices for AIDC barcoding solutions. However, users may also be looking for the interoperability of coding requirements for other AIDC methods, e.g. Radio Frequency IdentificationIf you've previously employed a previous version of this document, and are continuing to work in the same field of activity we strongly recommend buying this document, which has updated recommendations and international guidelines. Check out the most popular cen catalog standards en-1367-1-2007 review.

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Старый 13.10.2021, 20:58   #6
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По умолчанию ISO Standardization Is A Crucial Element To The Growth Of Your Business

Part 1: Safety Requirements And Essential Performance For Electrical Medical Equipment. Collateral Standard - Electromagnetic Disturbances. Tests And Requirements En 60601-1-2:2015
The design of medical equipment is more complicated and requires a greater understanding. Every medical system will have its own set of standards. This document applies to the safety and essential performance for Medical Equipment (ME), and ME Systems that are exposed to electromagnetic disturbances. The initial part of the standard provides an overview of the safety requirements in the use of medical equipment. See the most popular iso catalog standards iso-21597-2-2020 info.

Innovation Management - Innovation Management System - Guidance (Iso 56002:2019) En Iso 56002:2021
Innovative management systems are crucial for building a productive business structure. This is why it's so important to be attentive to the regulations that govern it, from its beginning to its final phase. EN ISO 56002: 2021 is just one of them.This document gives guidance on the design, maintenance, improvement, and continued development of an innovative management program for all established organizations. It can be used for:A) Organisations that want to sustain success through developing and demonstrating their capability to effectively manage innovations activities to achieve the desired results.b) customers, users and other interested parties who want to have confidence in the new capabilities of the organizationC. Interestd parties and organisations that seek to improve communications between themselves through an conception of an innovation management plan.d. Providers of training in or assessment of innovation management and/or consulting for it;e. policymakers who seek to boost the effectiveness and efficiency of support programs aimed at enhancing the ability to innovate and improve the competitiveness of organisations and the development in society.1.2 The guidance contained in this document is generic and intended to be applicable to:an) All kinds of businesses regardless of their nature size, size or sector. The emphasis is on established businesses, with the understanding that both temporary and startups can benefit from following these guidelines in totality or in part;b. All types of innovations, e.g. Innovations of all kinds, including product, service and process.c. Any kind of approach (e.g. Both internal and external innovation, market, user technology, design-driven actions.It does not describe the specific functions of an organisation, but rather provides general guidelines. It does not provide the tools or methods used or requirements for innovation activities.If you are confused by some of the modifications in this document, we suggest you speak with an expert to verify whether the international standard is suitable for implementation within your organization's current structure. Check out the best sist catalog standards sist-en-301-893-v2.1.1-2017 site.

The Characterisation And Determination Of Bulk Material And Crystal Silica Content. Part 1. General Information And Selections Of Testing Methods EN 17289-1:2020
Regulations are complicated both locally and internationally because of the wide range of materials used in production. International standards are currently being established to ease the process for companies and organizations that want to enter new markets.This document describes the requirements for the determinations of the size weighted fine fraction (SWFF) and the size weighted fine fraction crystalline silicon (SWFFCS).This document gives also guidance regarding how to prepare the sample as well as determination of crystallized silica through the X-ray powder diffractometry (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR).EN 17289-2 specifies a method to calculate the size-weighted fine fraction from a measured particle size distribution and assumes that the particle size distribution of the crystalline silica particles are the same as the other particles found in the bulk material. EN 1789-3 describes the liquid sedimentation process to determine the size weighted fine fraction of crystal silica. The two methods are based on certain limitations and assumptions, which are listed in EN 17289-2 and EN 1789-3, respectively. The method in EN 1789-3 could be applied to other constituents than CS when it is investigated and validated.This document is suitable for crystalline silica containing bulk material, provided it has been thoroughly researched and validated to allow for the analysis of size-weighted fine fractions and crystal silica.If your field of work comes into close contact with any of the materials described in this document, having it included in your technological documentation base will greatly aid the process of increasing production. The link to our site gives more information. Check out the top rated iec catalog standards iec-62209-2-2010 info.

Software Engineering And Systems. Software Product Quality Requirements Evaluations And Evaluations (Square) For Software Products. Common Industry Format (Cif) For Usability User Specifications (Iso 25065.2019). EN ISO 25065:2020
The most important advantage a business has in a competitive market is the quality of its software. There are specific rules for these markets which must be adhered to in the present. These requirements are contained in documents like EN ISO 25065 2020.This document provides a uniform framework and consistent terminology for defining specifications. This document outlines the industry standard (CIF) for specifications for user requirements, including the content elements, as well as the format used to describe them.A specification of the user's specifications is the official documentation of a user's requirements. This helps in the creation and evaluation of interactive systems.This document defines the requirements of users as the following: a. Interaction requirements for users with the system to attain the intended results (including specifications and attributes for the outputs of the system and their attributes); 2. Use-related quality requirements that define quality requirements in relation to the results of users interacting in the software interactively and may be applied to the system acceptance requirements.ISO/IEC 25030 introduces the concept of quality requirements. These are the types of quality requirements. The elements that constitute the specification for user requirements are designed to be used in documentation resulting both from activities listed in ISO9241-210 and human-centered design methods such as ISO9241-220.This document is designed to be used as a reference for business analysts, requirements engineers as well as product managers. It could also be used by product owners who are acquiring systems from third party vendors. The CIF series of standards addresses information on usability (as defined in ISO 9241-11 as well as ISO/IEC TR 25060).In addition to usability, user requirements could also be viewed from other angles, such as human-centred quality which is a feature of ISO 9241-220, as well as other quality-related perspectives that are presented in ISO/IEC 25010and ISO/IEC TS 25011 and ISO/IEC 25030.This document was developed for interactive systems however the guidance can be used in any area. The document is not a guideline for any process, method or lifecycle. It is possible to use the content elements of a user requirement specification in iterative design. This can include the elaboration or evolution of requirements. as in agile development).
Utilizing this international standard will significantly facilitate your professional activity as well as help you structure the existing system, and create the possibility of gaining new markets and scaling your business. See the most popular iec catalog standards iec-62396-2-2017 blog.

Health Informatics- Device Interoperability. Part 20701 - Point-Of-Care-Based Medical Communication. Service Oriented Medical Devices Exchange Protocols And Architecture. (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
The use of communication technologies is not just in the fields which are typically connected to this particular category as well as in the medical industry. The introduction of different medical devices require a complex restructuring. To make these processes easier, international documents have been developed.
This standard covers the architecture of medical devices that is service-oriented and the communication protocol specification for distributed systems that comprise PoC medical devices as well as IT systems that require the exchange of data or the safe supervision of PoC medical devices. It defines the functional elements and their communications.The document is specific and has been narrowly focused. We recommend to learn more about its technical parameters and consult the managers who are experts in international document selection. Have a look at the top rated clc catalog standards en-61229-1995 information.

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Старый 23.11.2021, 08:21   #7
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Старый 25.11.2021, 03:50   #8
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Старый 30.11.2021, 03:30   #9
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Старый 30.11.2021, 09:48   #10
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What are the major advantages of Autonomous Mobile Robots

1. Greater Flexibility
Since Autonomous Mobile Robots rely heavily on cameras and sensors onboard to function--not magnetic tape or wires like AGCs and AGVs--they are an example of flexibility and agility in automation. Autonomous Mobile Robots don't need to follow predetermined paths. They can instead design their own efficient routes within the facility. This helps them avoid obstacles. This allows Autonomous Mobile Robots are able to carry out new tasks with relative ease, compared to other automation systems that generally take longer and more effort to program. Check out this Cross docking robot info for more.

2. Improved Safety
Autonomous Mobile Robots come packed with sensors and cameras. They are able to perceive and comprehend their surroundings. This lets them move efficiently within a space, without having to collide with people, product, infrastructure or other obstacles. In contrast, machines operated by humans like forklifts do not have the same safety features and ultimately rely on input from humans. Autonomous Mobile Robots eliminate the risk of human workers becoming tired or distracted and causing an accident. Employing Autonomous Mobile Robots for easily-repeatable tasks thus allows the operation to eliminate the risk of human error and drastically increase the security of the facility.

3. Rapid Implementation
Autonomous Mobile Robots are able to be operational during an operation within about four to six weeks dependent on the particulars of the operation. This is particularly true when the device is required to interface with the software for warehouse execution and picking. Even with the latest technology, this can take a remarkable amount of time. For comparison, a goods-to-person (G2P) system could take as long as a year to fully implement.

4. Scalability
Autonomous Mobile Robots have a simple implementation within a facility. You can follow modular deployment and add units as your company grows or changes. This means that you do not need to invest an enormous amount of money in the beginning. Instead of purchasing large quantities of Autonomous Mobile Robots they can be purchased one or two and later expand your fleet. The modular deployment will free money that you can use to pursue other initiatives while you evaluate the impact of Autonomous Mobile Robots on your business and decide on the next steps.

5. It is easy to travel between facilities
Some operations may not be willing to consider automated options when they are aware that a move into a new facility is imminent. This is a good option. The new system can be removed in two years. In such a scenario, Autonomous Mobile Robots can be used to bridge the gap in the interim. Because Autonomous Mobile Robots are relatively easy to install, they can also be transferred between facilities with relative ease, enabling automated processes even in the short run. This is a benefit to businesses seeking to set up temporary holidays.
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