Clinical Data and Results definition

Clinical Data and Results means all information, data, and results developed or obtained in connection with clinical trials conducted within the scope of this Agreement.
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Clinical Data and Results means all information, data and results developed or obtained in connection with clinical trials conducted under the Research Plan whether by intramural research scientists or extramural grantee or contract investigators.
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Clinical Data and Results means all information, data and results developed or obtained in connection with clinical trials conducted within the scope of the CRADA Research Plan whether by intramural research scientists or extramural grantee or contract investigators.
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Examples of Clinical Data and Results in a sentence

  • Collaborator’s exclusive access under subsection (a) above to Clinical Data and Results and Raw Data in NIH’s Possession and Control is dependent, however, upon Collaborator’s continued development and commercialization of the technology.

  • As described in the Intellectual Property Option to Collaborator and the NCI Standard Protocol Language, Clinical Data and Results and Raw Data will be provided exclusively to the NCI, the Collaborator and the FDA, as appropriate.

  • To the extent permitted by law, Clinical Data and Results and Raw Data will be made available exclusively to Collaborator, the NCI and the FDA, as appropriate and for use in obtaining pharmaceutic regulatory approval for the commercial marketing of Agent.

  • To the extent permitted by law and subject to the other provisions of Article 8 of this CRADA, NIH shall maintain all IND, Clinical Data and Results, and Raw Data in NIH’s Possession and Control as Proprietary and CONFIDENTIAL, and make them data related to NCI Protocol 00-C-0050 (P-92) available exclusively to the Collaborator, for its own use and for use in obtaining FDA approval for the commercial marketing of Subject Inventions and Agent products.

  • In the event that Collaborator discontinues development or commercialization of the technology without the transfer of its development efforts to another party, NCI retains the right to make the Clinical Data and Results and Raw Data in NIH’s Possession and Control available to another collaborator.

  • Costs associated with providing Clinical Data and Results or Raw Data to Collaborator in customized formats shall be borne by Collaborator.

  • Modify the first sentence in Article 12.3 as follows: The Collaborator agrees to hold the U.S. Government harmless and to indemnify the Government for all liabilities, demands, damages, expenses and losses arising out of the use by the Collaborator for any purpose of the Subject Data, additional Clinical Data and Results and Raw Data in NTH’s Possession and Control.

  • Subject to the other provisions of Article 8 of this CRADA, NIH shall maintain, to the extent permitted by law, all IND, Clinical Data and Results and Raw Data in NIH's Possession and Control as Proprietary and CONFIDENTIAL, and make them available co-exclusively to RPRP and Introgen for each Party's (including sublicensees and affiliates) own use and for use in obtaining FDA approval for the commercial marketing of Subject Inventions and Agent products.

  • For clarity, CIMAC Data, Clinical Data, and Results from Cross-Trial Analysis will also be submitted to the controlled-access data archives or data commons described in 4(h) once the Cross-Trial Analysis has been published in manuscript form, for sharing with approved requestors from the general research community.

  • Finally, the IND, the Raw Data, and Clinical Data and Results generated by the clinical trials are being provided under this Agreement exclusively to Collaborator for use in Agent's anticipated commercialization and, therefore, shall not be shared or transferable to any third party without the written permission of the NCI.


More Definitions of Clinical Data and Results

Clinical Data and Results means all the clinical information, data, and results developed or obtained in connection with the Study. “CLIA refers to the Clinical Laboratory Improvement Amendments (CLIA) of 1988 under which the Centers for Medicare and Medicaid Services regulates all laboratory testing (except research) performed on humans in the United States (xxxx://xxx.xxx.xxx/Regulations-and-Guidance/Legislation/CLIA/index.html?redirect=/clia/)
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Clinical Data and Results means all information, data and results developed or obtained in connection with clinical trials conducted within the scope of the CRADA Research Plan whether by intramural research scientists or extramural grantee or contract investigators. 2.16 “Clinical Data and Results and Raw Data in NIH’s Possession and Control” means all information collected from NIH intramural preclinical or clinical studies performed pursuant to the Research Plan, all data obtained by NIH under contracts with extramural contract investigators for completion of studies within the scope of the CRADA Research Plan, and all information and data in the NCI-sponsored IND for Agent.
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Related to Clinical Data and Results

  • Clinical Data means the information concerning the safety or performance that is generated from the use of a device and that are sourced from the following:

  • Project Results means all data and results of the Project.

  • Research Results means any technical result acquired based on the Collaborative Research, including, but not limited to, any invention, idea, design, copyrightable work and know-how which relates to the purpose of the Collaborative Research.

  • Research Data means documents in a digital form, other than scientific publications, which are collected or produced in the course of scientific research activities and are used as evidence in the research process, or are commonly accepted in the research community as necessary to validate research findings and results;

  • Technical data means recorded information, regardless of the form or method of the recording, of a scientific or technical nature (including computer software documentation). The term does not include computer software or data incidental to contract administration, such as financial and/or management information.

  • Peer-reviewed medical literature means a scientific study published only after having been critically

  • Development Data means all non-clinical, clinical, technical, chemical, safety, and scientific data and information and other results, including relevant laboratory notebook information, screening data, and synthesis schemes, including descriptions in any form, data and other information, in each case, that is generated by or resulting from or in connection with the conduct of Development of Products.

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Study Data shall have the meaning set forth in Section 8.1.

  • Historical data means any data collected by an ALPR system and stored on the statewide ALPR server operated by the Vermont Justice Information Sharing System of the Department of Public Safety. Any data collected by an ALPR system in accordance with this section shall be considered collected for a legitimate law enforcement purpose.

  • Third Party Data has the meaning set forth in Section 9.3(a).

  • Dataset means the data specified in Appendix 1 (Environmental Information) to Schedule 11.2 (Management Information) as the same may be amended from time to time by the Secretary of State (acting reasonably);

  • Controlled technical information means technical information with military or space application that is subject to controls on the access, use, reproduction, modification, performance, display, release, disclosure, or dissemination. Controlled technical information would meet the criteria, if disseminated, for distribution statements B through F using the criteria set forth in DoD Instruction 5230.24, Distribution Statements on Technical Documents. The term does not include information that is lawfully publicly available without restrictions.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Data means recorded information, regardless of form, the media on which it is recorded, or the method of recording.

  • SAP Technology Solution(s means SAP NetWeaver Foundation for Third Party Applications, SAP Business Technology Platform (excluding when used solely as a Connectivity App between an SAP Application and ERP), SAP Signavio Solutions and SAP Process Insights (including any renamed, prior and/or successor versions of any of the foregoing made generally available by SAP if any but excluding when any of the foregoing are used as a User Interface for ERP.

  • Input Material means all documents, information, representations, statements and materials provided by Customer or a third party on behalf of Customer, relating to the Services, including computer programs, data, logos, reports and specifications and inventories.

  • Marketing Materials has the meaning ascribed thereto in NI 41-101;

  • Licensed behavior analyst means a person who holds current certification or meets the standards to be certified as a board certified Behavior Analyst or a board certified Assistant Behavior Analyst issued by the Behavior Analyst Certification Board, Inc., or any successor in interest to that organization and whom the Board of Psychological Examiners licenses as a Behavior Analyst.

  • Clinical peer means a physician or other health care professional who holds a non-restricted license in a state of the United States and in the same or similar specialty as typically manages the medical condition, procedure or treatment under review.

  • Product Data are illustrations, standard schedules, performance charts, instructions, brochures, diagrams, and other information furnished by the Contractor to illustrate materials or equipment for some portion of the Work.

  • GLO Data means any data or information owned by the GLO, including PII or SPI as defined below, that Provider creates, obtains, accesses (via records, systems, or otherwise), receives (from the GLO or on behalf of the GLO), or uses in the performance of the Contract or any documents related thereto.

  • Third-party filer means an entity that submits a Product filing to the Commission on behalf of an Insurer.

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • Licensed Programs means, collectively, NeoSystems’ and any Third Party Vendor computer software programs to be provided to Client for use on certain hardware on Client’s premises or a third party’s premises as set forth in an Agreement. The Licensed Programs shall include any fixes, work-arounds, updates, revisions, modifications, enhancements and any derivative works that are provided to Client by NeoSystems under an Agreement.

  • Third Party Material means software, software development tools, methodologies, ideas, methods, processes, concepts and techniques owned by, or licensed to a third party and used by the Service Provider in the performance of the Services;