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FIDIC Claims course online
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أدوات الموضوع | انواع عرض الموضوع |
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06-08-2020, 04:28 PM
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FIDIC Claims course online
Gentlemen: training Department The International Training &Consultation Center is pleased to invite you to attend the training program, the information required are in the following: FIDIC Claims: Management of Claims and Resolution of Disputes Objectives • Understand the claim and dispute resolution procedures under FIDIC Conditions of Contract • Recognize practical issues encountered on projects as to claims and disputes, and how to address those • Summarize recent FIDIC case law and other authorities as to claims and dispute matters • Apply practical/hands-on feedback and insights from an experienced FIDIC practitioner and a claims consultant • Demonstrate the necessary knowledge, advice and insights in order to navigate through the FIDIC claim and dispute provisions on their projects Course outline • Introduction to FIDIC • General Introduction • Introduction to the FIDIC Contracts • Managing Variations • Variations covered by Clause 13 and related clauses • Definition • Initiation and instruction of variations • Role of the Engineer • FIDIC approach (Construction versus Plant and Design-Build Contract) • The Management of Claims • Claims: causes and risks • Inherent project risks • Allocation of risks under FIDIC contracts • Analysis of contractual risk • Notices and claims procedures • Clauses requiring notice by the Contractor • Employer’s/Engineer’s claims (Sub-Clause 2.5) • Delegation by the Engineer (Sub-Clause 3.2) • Contractor’s claims (Sub-Clause 20.1) • Notification of claims • Contemporary records • Preparation of claims • Engineer’s assessment and principles of claim • Engineers valuation • Engineer’s determination (Clause 3.5) • Claims for delay • Extension of time (Sub-Clause 8.4 and 8.5) • Force majeure (Sub-Clause 19.4) • Delay damages • Claims for additional payment I • Ground conditions (Sub-Clause 4.12) • Late possession (Sub-Clause 2.1) • Breaches of contract • Employer’s financial claims • Procedure • Delay damages • Defects in works and/or design • Defects in work and design • Retention and bonds • The Responsibilities of the Main Parties • General Issues • The Employer • The Engineer • The Contractor • Termination by the Employer • Suspension and Termination by the Contractor • Risk and responsibility • Force majeure • The Resolution of Disputes • Dispute Adjudication Board (DAB) principles • Types of DAB • Guarantees and general obligations of the DAB • Nomination of DAB • Qualifications and selection of members • Cost and Payments to the DAB • Dispute Adjudication Board working • Appointment Failure to agree Referral to the DAB • Presentation of evidence to the DAB • The DAB’s decision • Post-DAB decision processes • Implementation • Post-DAB mediation • Enforcement • Amicable settlement • Arbitration • Arbitrating Claims • ICC Rules • Selecting arbitrators • Use of experts FIDIC Claims: Management of Claims and Resolution of Disputes • Registration & Contact information • Please sent confirmation letter for attending, to the following contacts: amal@itcegy.com Amal abdulrhman Training Advisor 00201110056192 If you would like any further information, please don't hesitate to contact me Training Advisor| amal abdulrhman Mob| 00201110056192 E-Mail| amal@itcegy.com With respect 
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08-30-2021, 12:45 AM
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رقم المشاركة : [2] | ||
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Keren Genset Kubota Halaman
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09-28-2021, 06:26 PM
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رقم المشاركة : [3] | ||
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10-12-2021, 04:32 PM
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رقم المشاركة : [4] | ||
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10-13-2021, 06:34 PM
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رقم المشاركة : [5] | ||
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ISO Standardization Is An Essential Step In Your Business's Development
Part 1-10: Medical Electrical Devices - General Requirements For Safety And Essential Performance – Collateral Standard Requirements To Create Closed Circuit Physiologic Controllers. En 60601-1-10:2008 For the safety of all medical equipment, it's crucial to have separate information. Standards are not only created to ensure the process of usage as well as to guarantee that the products are of high quality. That means that the awareness of the latest standards for medical equipment is at the same level as the general ones. EN 60601-1-10.2008 sets out the requirements for developing (analysis of design, verification of design and validation of a controller used in a closed-loop physiologic control system in medical electric equipment as well as medical electrical systems to regulate the variable. This collateral standard is applicable to all types and models of PCLC. If you're interested in the document mentioned, contact Iteh. Check out the top cen catalog standards cr-10313-2000 information. Innovative Technologies As A Topic To International Standardizations Innovative technologies are sweeping across the world. Every day, every second, a brand new device, or a new approach to applying technology that is already in use, is invented. The world is definitely changing as a result. The human condition is affected by the proliferation of electronic devices, communication and artificial intelligence. It's entirely possible that the entire world suffers from the failure to keep these devices in order. It is also important to not forget that with the development of the Internet and the speed of methods for transferring information, the number of risks of information leakage has increased and the issue of security becomes more and more relevant every day. Today we will provide information on the technical aspects of where and how to use these techniques in conjunction with the international standards that are responsible for data security. Check out the recommended 53.020.99 catalog ics review. Characterization Of Bulk Material - The Determination Of A Size-Weighted Fine Fraction Or Crystalline Silicon Content - Part 3. Sedimentation Method EN 17289-3:2020 There are a variety of ways to use to make and make utilization of various materials. Each of these techniques requires some level of regulation according to the specific activity. One of the documents that defines the precise method of application for crystalline silica is EN 17289-3: 2020.This document outlines the determination of the size-weighted fine portion (SWFF) and the size-weighted fine portion of crystallized silica (SWFFCS) in bulk materials, using the sedimentation technique employing a liquid sedimentation method.The aim of this document is to permit users to assess bulk materials with regard to their size-weighted fine fraction as well as the content of crystalline silica.This document is applicable to crystallized silica with bulk material that has been rigorously studied and verified for the evaluation of the size-weighted, fine fraction and the crystalline silica.Specification of production techniques simplifies the process for building the control system. If you're interested in expanding your market share we suggest you purchase international standards for your facility. Have a look at the recommended cen catalog standards en-12662-2014 review. Software Engineering And Systems. Software Product Quality Requirements And Evaluation (Square). Common Industry Format For Usability (Cif). Specification For User Requirements Specification (Iso 25065.2019). EN ISO 25065:2020 A company's main advantage in a competitive market is the quality of its software. In order to understand the regulations of these markets, it's essential to know the international standards that must be followed in the present. These standards are contained in documents like EN ISO 25065 2020.This document provides a uniform framework and terminology for defining user requirements. It defines the industry standard format (CIF) for a user requirement specification including the content elements as well as the format to express the requirements.A user requirements specification outlines the formal documentation and requirements of an item. It is utilized to aid in the creation, evaluation, and maintenance of interactive software that is usable.This document defines user requirements as follows. Requirements for interaction between users and systems to achieve intended outcomes (including specifications and attributes for the outputs of the system and their characteristics) 2. Quality requirements related to use which define quality standards in relation to the results of users who interact with the interactive software and can be applied to system acceptance criteria.ISO/IEC 25030 introduces a notion of quality requirements. They are the kind of quality requirements. The content elements of specifications for user requirements are designed to be used as part of the documentation that is derived from the processes described in ISO 9241-210, and from human-centered design processes similar to those found in ISO 9241-220.This document is intended for requirements engineers and product managers, as well as the product owner, and business analysts who are responsible for acquiring systems from other parties. CIF is a collection of standards that addresses usability-related information, as described in ISO 9241-11 or ISO/IEC TR 25060.They are not only usable however, they also offer different perspectives. ISO 9241-220 introduces human-centred qualities. Other perspectives on quality are presented in ISO/IEC 25010 and ISO/IEC TS 25011.Although this document was written to be used in interactivity, it could be used in other areas. This document doesn't prescribe any process, method or lifecycle. The content elements of the user requirements specification may be used in iterative development, which involves the development and refinement of requirements (e.g. as in agile development). The use of this international standard will significantly improve your professional work as well as help you create a structure for your current system and open up new opportunities for conquering new markets and expanding your business. See the top rated clc catalog tc clc-tc-64 information. Health Informatics Interoperability Of Devices. Part 101: Point Of Care Medical Device Communication. Domain Information Model. Iso/Ieee 11073-10201:2020. EN ISO/IEEE 11073-10201:2020 Documents related using medical devices are similar to the other standards. There are numerous components which can be used in conjunction with each other and discuss completely different technologies. EN ISO 1073/10201 IEEE 2020.The goal of this research is to define a general object-oriented model of information that could be used to arrange data and distinguish services utilized in points-of-care (POC) medical device communications. The scope of the project is mostly focused on medical equipment for acute care and the vital sign for communication of patients information.The use of information technology is increasing to improve business operations and boost productivity. We recommend that you think about purchasing documents that standardize their use worldwide. Check out the top sist catalog standards sist-din-5034-6-1997 information. |
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10-13-2021, 07:36 PM
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رقم المشاركة : [6] | ||
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ISO Standardization As A Key To The Growth Of Your Business
Part 1-9 Of Medical Electrical Equipment - General Requirements For Safety And Fundamental Performance - Collateral Standard Requirements For Environmentally Conscious Design En 60601-1-9:2008 Environment stands for the life of everyone on Earth. Although technology is constantly improving The main objective is to make sure that new systems remain safe. The new standards that regulate environmental safety in medical equipment were created to address this issue. The objective of this collateral standard is to enhance the environmental impact for the entire spectrum of medical equipment, considering all phases of the product's life cycle The process includes: - specification of the product design; manufacturing and distribution; logistics, sales, installation; - use; - the management of end-of-life. This is concerned with protecting the human health, the environment and the natural resources from hazardous substances. It also means conserving energy and raw materials by minimizing waste creation, and minimising adverse environmental impacts. This objective must be considered at all stages of medical equipment's life-cycle from design to end-of-life management. More information about this document on the website. Have a look at the recommended clc catalog standards en-60444-8-2017 blog. Innovation Management - Tools And Methods For Partnership In Innovation - Guidance (Iso 56003-2019) En Iso 56003:2021 When it comes to the development of new products one of the primary functions is the development of a suitable partnership through which it is possible to exchange technologies, recommendations in support of resource and financial support in addition to many other important aspects for creating a developing system. EN ISO 56003: 2021 is one of the international standards that outlines how to form productive partnerships.This document is intended to provide guidance for partnership models for innovation. It offers instructions on how to establish partnership in the field of innovation.Choosing whether or not to join an Innovation PartnershipIdentify, evaluate, and select partnersEnsure that the partners have similar views of the value and the challenges they face.Manage the partner interactions.The advice provided by this document is applicable to any kind of partnership and collaborations and it is intended to be useful to all organizations, regardless of its type, size, product/service provided, such as  a) Startups work with larger corporationsB. Medium and small enterprises (SMEs) or larger corporations;c) private sector companies that have public or academic entities;D. Academic, public and non-profit organizationsBegin with a gap analysis first, then identify and engage potential innovation partners, and then, manage their interactions.This standard can be used by both small and large companies, as well as novice startups. Partnership is a crucial element that will drive profitable growth and expansion in the future. This is why we recommend you pay close attention to this document if your organization is focused on growth for the long term. Check out the top rated clc catalog standards en-61440-1997 site. The Characterisation Of Bulk Materials - Determination Of An Amount-Weighted Fine Fraction, And The Content Of Crystalline Silica - Part 3: Sedimentation Technique EN 17289-3:2020 There are a variety of methods used to make and use various materials. Each method requires a specific amount of regulation based on the amount of work involved. EN 17178-3: 2020 is one of the documents that define the application methods for the crystalline silica.This document outlines how to determine the size-weighted fine portion (SWFF) and the size-weighted fine fraction of silica crystalline (SWFFCS) in bulk materials using a sedimentation method using a liquid sedimentation technique.This document is meant to aid users in evaluating bulk materials on the basis of their size-weighted fine fraction or crystalline silica.This document covers crystallized silica with bulk material that has been thoroughly investigated and verified for the evaluation of the size-weighted, fine fraction as well as the crystalline silica.The specification of manufacturing methods allows you to create a control network. If you're planning to increase your market share we suggest you purchase international standards for your facility. See the best cen catalog tc cen-ws-bii2 review. Machine Tools Safety – Safety For Presses Part 4 : The Safety Requirements Of Pneumatic Presses. (Iso 16092-4.2019). EN ISO 16092-4:2020 Safety issues are an essential aspect of creating a regulatory framework for any business or production. That is why there is a wide range of international standards which address this issue.This document, along with ISO 16092-2, provides technical safety requirements which must be adhered to by everyone who is accountable for the design, development and delivery of pneumatic presses that are designed to operate with cold metals, or materials partly made from cold steel.This document outlines all dangers associated with pneumatic presses. They are intended to be used under conditions that are reasonably predicted by the manufacturer. Each of the phases that make up the life of the machine as defined in ISO 12100.2010, 5.4 were taken into account.If you're looking to purchase this document, you can always clarify all of the technical specifications by clicking on the link to our site, as well as contact our team to with the details you are interested in. Have a look at the top rated cen catalog standards en-16341-2012 info. Health Informatics -Standard Communication Protocol Computer Assisted Electrocardiography EN 1064:2020 Despite the fact the introduction of technology in medicine took place in the past decade, it has been much more rapid in recent times. This is due to the fact that technological advancement and innovation are primarily focused in the medical sector. Security of information is an essential element of this business because it is responsible for human safety. This is why EN 1064:2020 is a global standard.This document describes the standard guidelines for cart to cart exchange and cart-to-cart exchange of patient information. This document details the content and format of the data that will be transferred between digital ECG Carts as well as computer ECG Management Systems, and other systems on computers where ECG data is stored.You will see a huge improvement in your company's capability to compete in today's market when you follow this standard. Click on the hyperlink below to learn more details about the standard. Check out the recommended cen catalog standards pren-1176-10 blog.  |
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