Research Data. During the 45 DAY EXPERIMENT I will be asked to provide personal; psychological, including but not limited to written and narrative data and responses on psychological measures; and biophysical data, including but not limited to brain wave, heart rate, and galvanic skin response measurement and data (collectively ‘Data’) by the 45 DAY EXPERIMENT ORGANIZATION for ongoing research projects at the Center for the Study of Non-Symbolic Consciousness and the Transformative Technology Laboratory and their partner and affiliate researchers and organizations. I agree to abide by all data collection procedures specified in the 45 DAY EXPERIMENT. I acknowledge that any and all of said Data are the exclusive property of the Center for the Study of Non-Symbolic Consciousness and Transformative Technology Lab. I further acknowledge that the Center for the Study of Non-Symbolic Consciousness is the exclusive copyright owners of this Data. I shall have no claim, right or interest to any of this Data and my signature hereto grants permission to the Center for the Study of Non-Symbolic Consciousness to use said Data. I do hereby hold harmless and forever release the Center for the Study of Non-Symbolic Consciousness, Transformative Technology Lab, and 45 DAY EXPERIMENT ORGANIZATION and their licensees, agents and assigns from any claims arising from the use of said Data.
Research Data. If You are a Participant in a Research Project, You acknowledge that We will collect and generate Data from and in connection with the Research Project, including with respect to Your participation and the provision of the Microbiome Services to You (Research Data). This Research Data may include, without limitation, raw and analysed data, microorganism DNA xxxxxxxx xxxx, metagenome-assembled genomes (MAGs), genome metadata and survey metadata. You acknowledge and agree that, to the extent permitted by law, the Research Data will be owned by Us. To the extent that title to any Research Data does not or cannot vest in, or be assigned to, Us, You grant to Us a perpetual, irrevocable, world-wide, non- exclusive, royalty free and fee-free licence (with a right to sub- licence and assign) to use that Research Data for the purposes set out in the applicable Participant Information Sheet and any other purposes that We see fit. You acknowledge that Our use of any Research Data may be subject to any agreement We may have with Our Research Partners. You acknowledge that You will not acquire any rights in any works or research or commercial products that may be discovered, developed or derived by Us or Our licensees from any Research Data. All such rights are owned by Us or Our licensees (as the case may be). Intellectual Property We and our licensors (as applicable) own all Intellectual Property in Microba (including without limitation text, graphics, architecture and coding and any copyright subsisting in them). We own all trade marks, branding and logos contained in, or relating to, Microba and you cannot use them for any purpose without our express written consent. Without limiting the above, all Intellectual Property rights in all Microbiome Reports are owned by Us. If We provide You with a Microbiome Report as part of the Microbiome Services, You may access and download Your Microbiome Report and may disclose such information to family and medical professionals for the purposes of obtaining medical advice, however You must not modify, publish, transmit, distribute, participate in the transfer or sale, create derivative works, or in any way exploit, Your Microbiome Report in whole or in part without Our prior written permission. Outcomes and reliance on information Nothing contained in any Microbiome Report or on Our Website should be construed as medical advice. Any information We provide to You (including information set out in Your Microbiome Report or on Our...
Research Data a. Data management is good scientific practice, ensuring that research can be verified, reproduced, and reused5. For that reason, creating a Data Management Plan (DMP) should be an integral first step of every research project. DMPs are living documents requiring revisions and updates as research progresses 6. The following aspects are usually covered: data collection and description; metadata; storage and archiving; legal considerations and usage6.
b. Crucial for the reuse of any data either by the creator or any other scientist is clear and consistent labeling and documentation of data and metadata.
c. All research data and results must be reliably retained and stored for ten years. It does not matter whether the research results are published or not3. MPI-AB is providing the required infrastructure to guarantee that information stored both digitally and in analog format is secured and remains accessible3.
d. Archiving beyond the obligatory ten years of storage aims particularly at possible later use in different contexts. This long-term archiving is restricted to the meaningful part of the data and metadata3.
e. The Xxx Xxxxxx Digital Library (MPDL) provides tools and training for all these aspects from generating DMPs to long-term archiving and publication of research data 7.
f. Project participants who substantially contributed to collecting the data or made key contributions to their processing, may make use of the data and possibly take a copy of the data with them. If several persons can claim an entitlement to the data, they must all be considered as authorized to use the data, except where this would put at risk the success of the research project for which the data were collected. If data can only be used in one single research project for compelling material reasons, it must be assumed that the authorization for its use lies with the people/person who primarily collected it and their project(s)3.
g. In the case of research projects and especially cooperation projects involving several institutions, it is advisable to conclude documented rights of use agreements for all project participants at the earliest opportunity3. 5 xxx.xxxx.xxx.xx/xxxxxxxxxxxx/xxxxxxxx-xxxx-xxxxxxxxxx/ 6 xxx.xxxx.xxx.xx/xxxxxx-xxxxxxxx/xxxx-xxxxxxxxxx-xxxxx/ 7 xxx.xxxx.xxx.xx/
Research Data. The Contractor must seek and obtain prior written authorization from CMS and the Department for the use of any data pertaining to this Contract for research or any other purposes not directly related to the Contractor’s performance under this Contract.
Research Data. During the NEXT LEVEL CHALLENGE I will be asked to provide personal; psychological, including but not limited to written and narrative data and responses on psychological measures; and biophysical data, including but not limited to brain wave, heart rate, and galvanic skin response measurement and data (collectively ‘Data’) by the NEXT LEVEL CHALLENGE ORGANIZATION for ongoing research projects at the Center for the Study of Non-Symbolic Consciousness and the Transformative Technology Laboratory at Sofia University in Palo Alto, CA and their partner and affiliate researchers and organizations. I agree to abide by all data collection procedures specified in the NEXT LEVEL CHALLENGE. I acknowledge that any and all of said Data are the exclusive property of the Center for the Study of Non-Symbolic Consciousness and Transformative Technology Lab. I further acknowledge that the Center for the Study of Non-Symbolic Consciousness is the exclusive copyright owners of this Data. I shall have no claim, right or interest to any of this Data and my signature hereto grants permission to the Center for the Study of Non-Symbolic Consciousness to use said Data. I do hereby hold harmless and forever release the Center for the Study of Non-Symbolic Consciousness, Transformative Technology Lab, and NEXT LEVEL CHALLENGE ORGANIZATION and their licensees, agents and assigns from any claims arising from the use of said Data.
Research Data. All SHDF Research Data collected in addition to that essential to deliver SHDF Wave 2.1 are processed on a consent-only basis. They are subject to a maximum retention period of 7 years after the completion of the research. Please note: the Authority’ research partners for SHDF Wave 2.1 are yet-to-be appointed. Aspects of this are subject to change. Name of Lead LA Text Name of Lead Local Grant Recipient, whether it is a consortium application and if so all other Registered Providers of Social Housing involved in the application. Summary of status Drop-down Please provide a RAG rating on how the project is performing Activities this period Text Describe the current state of play of the project. Outline activities undergone by the LA during this reporting period Plan for next period Text Outline what activities are planned for the next reporting period Estimated Project Completion date Date Insert when you estimate the project will be complete. Date at which project team was appointed Date MS1 – Insert the date when the full project team is appointed Procurement activity stage completion date Date MS2 – Insert the date when all your projects complete their procurement activity Pre-construction tenant engagement completion date Date MS3 – Insert the date when all pre- construction tenant engagement is complete PAS2035 Risk Assessment stage completion date Date MS4 – Insert the date when all projects complete the PAS2035 risk assessment stage PAS2035 Dwelling Assessment stage completion date Date MS5 – Insert the date when all projects complete the PAS2035 dwelling assessment stage Design & Coordination completion date Date MS6 – Insert the date when all projects complete the design and coordination stage Installation stage started Date MS7 - Insert the date that installation starts Installation stage completed Date MS8 - Insert the date that all projects finish installing measures Handover and data lodgement completed Date MS9 – Insert the date that all projects complete handover and data lodgement stage Top 5 Risks Text Risks descriptions, category, mitigation, RAG of the top 5 risks Instances of Fraud Text Instances, mitigation, RAG Total Number of Installers Number Provide the total number of installers cumulatively that have worked on the project Total Number of Apprentices Number Provide the total number of apprentices cumulatively that have worked on the project % of Project Team Appointed % Outline the percentages of the project team that has been appo...
Research Data. 8.1 An important national research asset is the data and meta-data hosted and controlled by Institute ROs and associated partners. The University will, and will procure that each of the other Site ROs will, use their best endeavours to work with this distributed data asset network as expert data users and in accordance with the requirements of the relevant data Controllers (as such term is defined in clause 11.3). The University will, and will procure that each of the other Site RO’s will, support Institute activities by endeavouring to enhance data asset availability, quality, comparability and new data asset creation, for example asset and metadata cataloguing, documentation of data standards, data dictionaries, ontologies, and meta-data convergence. Site RO’s who are data Controllers will be expected to share data assets and facilitate access between Substantive Sites and Partnership Sites and across Institute researchers in as seamless a way as possible.
8.2 HDR UK Ltd will develop a single, consistent and transparent framework for the ethical and legal research use of data assets within the Institute. The University will, and will procure that each of the other Site ROs will, adopt this framework, incorporating the governance, data sharing and public engagement approaches of the Institute.
8.3 The University will be responsible for:
8.3.1 the operation of a secure infrastructure for data management and data sharing at the Site, in compliance with all relevant regulations / legislation;
8.3.2 the provision of robust Site data stewardship, evidenced by organisational arrangements proactively governing data management and data sharing.
8.3.3 the Site’s professional and effective management of relationships and coordinating activity with partner data custodians e.g. local NHS Trusts and other healthcare data providers.
Research Data. 5.2.6.1. The Contractor must seek and obtain prior written authorization from CMS and DMAS for the use of any data pertaining to this Contract for research or any other purposes not directly related to the Contractor’s performance under this Contract.
Research Data. What to keep, FAIR in practice, Sowing the seed: Incentives and motivations for sharing research data, a researcher’s perspective and Directions for Research Data Management in UK Universities)
Research Data. “Research Data” shall mean the result of observations or experimentation that validate research findings and that are published separate to the Article, which can include but are not limited to raw data, processed data, software, algorithms, protocols and methods. With respect to any Research Data that I wish to make accessible on a site or through a service of Journal Owner, Journal Owner shall have a perpetual worldwide, non-exclusive right and license to publish, extract, reformat, adapt, build upon, index, redistribute, link to and otherwise use all or any part of the Research Data in all forms and media (whether now known or later developed), and permit others to do so. Where I have selected a specific end user license under which the Research Data is to be made available on a site or through a service, the publisher shall apply that end user license to the Research Data on that site or service.
