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 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.
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. Appendix D – List of Data Items to be Shared with the Authority Project Summary - Monthly Item Type Definition 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 wo...
Research Data. We may also administer surveys and questionnaires to Customers and authorized users, in order to better understand how they use our Services or for other research or analysis purposes (“Research Data”). Participation is completely voluntary. We will not request any personal information about students or parents as part of this Research Data.
Research Data. We may review and analyze Research Data in order to better understand how Customers use our Services, to develop aggregate reports and for other research or analysis purposes.
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. In accordance with Section 2.14 of this Agreement, Manager shall undertake research using certain clinical data assembled by Practice. Except where authorization for the use of Protected Health Information in research is obtained in accordance with the Federal Privacy Regulations, such clinical data shall be furnished to Manager in the form of a limited data set that meets the requirements of Section 164.514(e) of the Federal Privacy Regulations. That limited data set shall be used by Manager, and by its employees and agents, exclusively for the purposes of research, public health and health care operations. Manager also may grant access to the limited data set to other individuals or entities engaged in research activities. Manager shall not use or further disclose information contained in the limited data set other than as permitted by this Section 2.17(b) or as otherwise required by law. Manager further agrees that it will (i) use appropriate safeguards to prevent use or disclosure of the information contained in the limited data set other than as provided for in this Section 2.17(b), (ii) report to Practice any use or disclosure of such information not provided for in this Section of which it becomes aware, and (iii) ensure that any agents or subcontractors to whom Manager provides the limited data set agree to the same conditions and restrictions with respect to such information. Manager will not identify the information contained in the limited data set or use the limited data set to contact the individuals whose information is contained therein.
