Objective and background Sample Clauses

Objective and background. The objective of the deliverable at hand is to analyse the work performed and results achieved in WP2 and WP3 as of 2020-07-13. The objective is to identify key challenges, key opportunities and derive concrete key actions and implementation paths to xxxxxx the open science code of conduct in the European AAT community. By analysing the work and results of WP2 and WP3, we can align the OSCAR project more precisely with its main goal that is to show how open science can be integrated into European AAT research projects in the future. The deliverable D4.1 is an important step for the ongoing project process particularly for the development of the pilot version of the open science code of conduct (D4.3) as well as for the planned simulated integration of the code of conduct into selected European pilot projects (WP5).
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Objective and background. A. Objective 1 B. Background 2
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Objective and background. One of the main goals of work package 4 (WP4) is to develop an open science code of conduct for the European AAT research landscape. For this purpose, preparatory work had to be done to explore and define the appropriate content and structure of the open science code of conduct. Furthermore, it is important to have a concise and comprehensive roadmap that lays out all the necessary steps, activities and milestones. Based on our early planning at the beginning of the OSCAR project and based on insights from D4.1 we were able to develop such a roadmap. The key elements of this roadmap to OSCAR code of conduct are presented in D4.2 at hand.
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Objective and background. The objective of this agreement (“Agreement”) is to regulate the Parties’ rights and obligations regarding the processing of personal and health data in accordance with Norwegian law and the EU General Data Protection Regulation (“GDPR”), confer personopplysningsloven (Act on Processing of Personal Data of the 15th of June 2018 number 38) § 1 in conjunction with Article 28 number 3 of the GDPR. The Agreement shall ensure that no personal data is to be processed inappropriately or unlawfully and that confidentiality, integrity, availability, and resilience of the data is maintained during the assignment. The Agreement regulates the Processor’s processing activities on behalf of the Controller, hereunder among other activities collection, recording, structuring, storage, adaptation, alteration, retrieval, disclosure, erasure, and restriction of personal data, or any combinations of these. The main objective of the Processor’s processing of personal data on behalf of the Controller is to assist the Controller in complying with the Controller‘s legal obligation to report adverse events or reactions during clinical trials to the applicable supervisory agencies. Personal data processed on behalf of the Processor may not be used for purposes other than the delivery and management of information regarding reporting of adverse events or reactions without the Controller’s prior approval. The Processor shall not transfer personal data covered by this Agreement to anyone other than the Controller, except in accordance with this Agreement or a subsequent agreement between the Parties.
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Objective and background. The objective of this Agreement is to regulate the processing of personal data which the Processor is performing on behalf of the Controller. The Agreement regulates the Parties’ compliance with the Personal Data Protection Act and the General Data Protection Regulation with regard to the processing of personal data performed by the Processor on behalf of the Controller. The Agreement imposes upon the Parties all the rights and obligations required to comply with the Personal Data Protection Act and the General Data Protection Regulation. This Agreement is an integral part of the Processor’s Standard Conditions. The Agreement shall apply to the Parties when they are bound by the Processor’s Standard Conditions. The Processor may amend and update this Agreement unilaterally if all amendments and updates ensure compliance with current personal data protection legislation, including the Personal Data Protection Act, the General Data Protection Regulation and any subsequent personal data protection legislation. The Processor shall inform the Controller of any such changes. The purpose of the processing regulated by this Agreement is to provide access to and operation of the agreed services/products covered by the Standard Conditions. The Processor shall process the following types of personal data on behalf of the Controller: Location details for vehicles (GPS coordinates) and information deriving therefrom • Identification details for employees (names, ID numbers, allocated vehicles, contact details etc.) • Contact details (names, e-mails, addresses, telephone numbers etc. of persons/customers) • Registration details for vehicles • With regard to HealthCare: Location, identification and contact details for persons carrying monitored equipment [...] The Processor is assigned to process personal data within the following categories of data subjects: • Employees • Tenants and other customers, including children • Service providers The Processor has designed his systems so as – in principle – not to process sensitive data on behalf of the Controller.
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Objective and background. The objective of this agreement (“Agreement”) is to regulate the Parties’ rights and obligations regarding the processing of personal and health data in accordance with Norwegian law and the EU General Data Protection Regulation (“GDPR”), confer Act on Processing of Personal Data of the 15th of June 2018 number 38 § 1 in conjunction with Article 28 number 3 of the GDPR. The Agreement shall ensure that no personal data is to be processed inappropriately or unlawfully and that confidentiality, integrity, availability, and resilience of the data is maintained during the assignment. The Agreement regulates the Processor’s processing activities on behalf of the Controller, hereunder among other activities collection, recording, structuring, storage, adaptation, alteration, retrieval, disclosure, erasure, and restriction of personal data, or any combinations of these. The main objective of the Processor’s processing of personal data on behalf of the Controller is to assist the Controller in complying with the Controller‘s obligation to monitor the clinical trial NAME OF STUDY. Personal data processed on behalf of the Processor may not be used for purposes other than the delivery and management of information in connection to the performance of monitoring services without the Controller’s prior written approval. The Processor shall not transfer personal data covered by this Agreement to anyone other than the Controller, except in accordance with this Agreement or a subsequent agreement between the Parties.
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Objective and background 
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Related to Objective and background

  • Objective and Scope 1. The Parties shall aim at the liberalisation of current payments and capital movements between them, in conformity with the commitments undertaken in the framework of the international financial institutions and with due consideration to each Party's currency stability.

  • Purpose and Background 1.00─Purpose and Background

  • Project Background 6.1.1. Brief description of Contracting Agency’s project background and/or situation leading to this Project

  • BACKGROUND AND OBJECTIVES The partnership proposed by the Cooperator was selected due to merit review evaluations from the 2017 Notice of Funding Opportunity P17AS00037. The Cooperator demonstrated expertise in disciplines and subject areas of relevance to cooperative research and training. The Cooperator met the program interests of NPS with expertise, facilities, experience, diversity of programs, and history of collaborative research projects. The Cooperator helps the NPS-CESU to meet its objectives to:  Provide research, technical assistance and education to NPS for land management, and research;  Develop a program of research, technical assistance and education that involves the biological, physical, social, and cultural sciences needed to address resources issues and interdisciplinary problem-solving at multiple scales and in an ecosystem context at the local, regional, and national level; and  Place special emphasis on the working collaboration among NPS, universities, and their related partner institutions. Title: Provide research, technical assistance and education for resource management and research The CESU network seeks to provide scientifically-based information on the nature and status of selected biological, physical, and cultural resources occurring within the parks in a form that increases its utility for making management decisions, conducting scientific research, educating the public, developing effective monitoring programs, and developing management strategies for resource protection. Studying the resources present in NPS parks benefits the Cooperator’s goal of advancing knowledge through scientific discovery, integration, application, and teaching, which lead toward a holistic understanding of our environmental and natural resources. The Cooperator is a public research university, sharing research, educational, and technological strengths with other institutions. Through inter-institutional collaboration, combined with the unique contributions of each constituent institution, the Cooperator strives to contribute substantially to the cultural, economic, environmental, scientific, social and technological advancement of the nation. The NPS expects there to be substantial involvement between itself and the Cooperator in carrying out the activities contemplated in this Agreement. The primary purpose of this study is not the acquisition of property or services for the direct benefit or use by the Federal Government, but rather to accomplish a public purpose of support or stimulation authorized the Legislative Authorities in ARTICLE II. This agreement fulfills the Public Purpose of support and economic stimulation for the following reasons:  Projects will engage recipients, partners, communities, and/or visitors in shared environmental stewardship.  Projects will promote greater public and private participation in historic preservation programs and activities. The project builds resource stewardship ethics in its participants.  The information, products and/or services identified or developed by projects will be shared through a variety of strategies to increase public awareness, knowledge and support for historic preservation and stewardship of the nation’s cultural and historical heritage.  Projects will support the Government’s objective to provide opportunities for youth to learn about the environment by spending time working on projects in National Parks. The NPS receives the indirect benefit of completing conservation projects.  Projects will motivate youth participants to become involved in the natural, cultural and /or historical resource protection of their communities and beyond.  Students gain “real world” or hands-on experience outside of the classroom of natural, cultural and/or historical resource projects.  The scientific community and/or researchers external to NPS gains by new knowledge provided through research and related results dissemination of natural, cultural and/or historical resource information.  Projects assist in the creation, promotion, facilitation, and/or improvement of the public’s understanding of natural, cultural, historic, recreational and other aspects of areas such as ecological conservation areas, and state and local parks. For performance under this cooperative agreement, the regulations set forth in 2 CFR, Part 200, supersedes OMB Circulars A–21 (2 CFR 220), A–87 (2 CFR 225), A–110, and A–122 (2 CFR 230); Circulars A–89, A–102, and A–133; and the guidance in Circular A–50 on Single Audit Act follow–up apply. The Cooperator shall adhere to 2 CFR, Part 200 in its entirety in addition to any terms and conditions of the master agreement not superseded by 2 CFR 200, as well as the terms and conditions set forth in this agreement. In the event of a conflict between the original terms of the master agreement and 2 CFR, Part 200, relating to this task agreement, 2 CFR, Part 200 shall take precedence.

  • Background 1.1. The “Work” is the research article, review article, letter, clinical trial study, report, article, or other copyright work, as identified in the Copyright Letter and further detailed in Schedule 1: Details of the Work (including such form of the copyright work submitted to Xxxxxxx Science for publication pursuant to clause 4, below), but excluding (except where context otherwise requires) any diagrams, figures or illustration specifically identified to Xxxxxxx Science pursuant to clause 3.2, below.

  • Targets and Milestones You may choose to develop specific additional targets and milestones which assess your performance in ITT over time – particularly if ITT trainees make up a significant proportion of your overall student body. Alternatively, you may have targets and milestones in your existing 2012-13 access agreement which you now also wish to apply to undergraduate and/or postgraduate ITT trainees. These targets may be statistical – based on how representative your entrants are and/or your retention performance – and might include annual or interim milestones to help you monitor whether you are making progress. You may wish to include criteria around the numbers of trainees in receipt of a full or partial maintenance grant, as financial data will need to be collected to determine bursary support and the data will also be accessible through the Student Loans Company for HEBSS subscribers. You may also wish to consider the TDA guidance at Annex C which gives information on specific groups that are Annex A underrepresented in the teaching profession. In this section, please state whether you intend to develop additional targets and milestones, or the extent to which you intend to use targets and milestones in your existing agreement which you now wish to extend to apply to undergraduate and/or postgraduate ITT trainees. Where you have new or amended milestones and targets, you should set these out in your Excel template (Annex B) at Table 6. Existing targets will apply.

  • Background Screening VENDOR shall comply with all requirements of Sections 1012.32 and 1012.465, Florida Statutes, and all of its personnel who (1) are to be permitted access to school grounds when students are present, (2) will have direct contact with students, or (3) have access or control of school funds, will successfully complete the background screening required by the referenced statutes and meet the standards established by the statutes. This background screening will be conducted by SBBC in advance of VENDOR or its personnel providing any services under the conditions described in the previous sentence. VENDOR shall bear the cost of acquiring the background screening required by Section 1012.32, Florida Statutes, and any fee imposed by the Florida Department of Law Enforcement to maintain the fingerprints provided with respect to VENDOR and its personnel. The parties agree that the failure of VENDOR to perform any of the duties described in this section shall constitute a material breach of this Agreement entitling SBBC to terminate immediately with no further responsibilities or duties to perform under this Agreement. VENDOR agrees to indemnify and hold harmless SBBC, its officers and employees from any liability in the form of physical or mental injury, death or property damage resulting from VENDOR’s failure to comply with the requirements of this section or with Sections 1012.32 and 1012.465, Florida Statutes.

  • SCHEDULE AND MILESTONES The planned major milestones for the activities for this Annex defined in the "Responsibilities" Article are as follows:

  • Objectives and Scope 1. The Parties confirm their joint objective of strengthening their relations by developing their political dialogue and reinforcing their cooperation.

  • Introduction and Background 1.1 The purpose of this Schedule 2 (Contract Services and Contract Supplies) is to set out the characteristics of the Contract Services and/or Contract Supplies (as the case may be) and Funding that the Provider will be required to make available to all Contracting Authorities in relation to Lot 1 and/or Lot 2 (as the case may be) and to provide a description of what the Contract Services and/or Contract Supplies (as the case may be) and Funding will entail.

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