Research Studies Sample Clauses

Research Studies. This agreement does NOT cover research studies.
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Research Studies. Advise, prepare, manage and submit desktop studies and reports as prescribed by the Client. Prepare perspective sketches, 2D and 3D images for proposals, including presentation material for exhibitions and the press. Presentation materials to be in both hard copy and electronic formats; Research, advise and present impacts of emerging legislation and best practice guidance including sustainability issues; Assist the Client with the preparation of good practice guidance and research and help the Client promote of this material.
Research Studies. The GCDC occasionally hosts consultations and participation in research studies/photographs of children participating in Center activities, which have been approved by the Board of Directors. You will be notified of these occasions in advance and will be required to grant/deny permission for your child to participate.
Research Studies. Children and families referred to the SSCC for services will not participate in research and/or studies without the prior written approval of DFPS.
Research Studies. (a) Primary Investigators of research or program evaluation studies conducted by The Foundation that impact the daily activities of students, parents or staff, or require use of data from the same individuals must submit a Research Request to the District’s Institutional Review Board (IRB) for review and approval prior to the initiation of any study-related activities. The District’s IRB and Research Review Process reviews the design, procedures, and potential impact on school and district operations to ensure the following: 1) the purpose, scope, limitations, and duration of study is clearly outlined; 2) the protection of human subjects in the research process;
Research Studies. Facility shall obtain prior written approval from Tivity Health for any research or clinical studies of Members or the Program. Facility shall provide study findings and results to Tivity Health prior to any publication or presentation of such findings or results.
Research Studies. IIR projects (“Studies”) considered for support by Pfizer could include any of the following: a. Interventional clinical studies b. Prospective observational clinical studies c. Retrospective (records based) human subject research d. Preclinical studies (animal or in vitro)
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Research Studies. The parties devoted considerable attention to the subject of occupational health within groups of company employees represented by the Unifor. The company recognizes that there is value in health research and will pursue jointly with the Unifor proposals for occupational health and engineering control research studies by reputable institutes and/or universities. It was understood that such research would be funded by other than company sources. Such proposals shall be evaluated by the master health and safety committee. During 2005 negotiations, the parties discussed research protocols and the company confirmed that it will consider appropriate gender representation in all research projects that are conducted in facilities. During prior negotiations, the company agreed to provide the Unifor National Health and Safety Coordinator with copies of completed Occupational Health and Safety Research Projects conducted by the company in its U.S. facilities.
Research Studies. To the extent that the Development Plan includes any research study involving the use of clinical samples or clinical data that, in each case, are obtained, generated or developed thereunder, the Parties agree that each Party will disclose and transfer to the other Party any raw data it obtains or generates in performing those research studies (to the extent that it Controls such data) along with a final report containing key conclusions from that study.” 9. Section 11.11(c)(iii). Section 11.11(c)(iii) shall be amended by restating the entire subsection (iii) as follows: “Any Losses involving a Third Party products liability claim or Action (other than such Losses entitled to indemnification under subsection (c)(i) or (c)(ii)) shall (a) be borne by Millennium to the extent such Losses were incurred (x) with respect to the Development of the Product conducted by Millennium, except to the extent of any claims related to manufacturing or design defects of OBI, or any Product Manufactured by Millennium or (y) with respect to the Commercialization of the Product in the U.S. and (b) be borne by OBI to the extent such Losses were incurred (x) with respect to the Development of the Product conducted by OBI, except to the extent of any claims related to manufacturing or design defects of Millennium, or any Product Manufactured by OBI or (y) with respect to the Commercialization of the Product in the License Territory.”
Research Studies. The research studies to be performed by each Party during Collaboration Stage 1 are listed in Appendix 2. The studies to be performed in subsequent Collaboration Stages will be determined by mutual written agreement of the Parties prior to the start of such Collaboration Stage.
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