Research Studies. This agreement does NOT cover research studies.
Research Studies. Advise, prepare, organise and submit desktop studies and reports; Prepare perspective sketches, images for proposals including presentation material for exhibitions and the press. Presentation materials to be prepared in both hard copy and electronically; 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 in the promotion 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:
Research Studies. IIR projects (“Studies”) considered for support by Pfizer could include any of the following:
Research Studies. (a) Primary Investigators of research or program evaluation studies conducted by AIR 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:
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. Agency agrees that prior to using the Equipment for a research study or publishing any results from such a study, the Agency will obtain AMS’ prior written approval of the study and additional written approval of any intent to publish the research results. AMS may, at its sole discretion, withhold any such approval. Agency’s breach of this Section 6.4 will be a material breach of the Agreement.
Research Studies. The research studies conducted by or on behalf of, or sponsored by, the Company or its current Subsidiaries, or in which the Company or its current Subsidiaries have participated, that are described in the Registration Statement, General Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, General Disclosure Package or the Prospectus, as applicable, were and, if still pending, are being, conducted in all material respects in accordance with applicable experimental protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company or its current Subsidiaries and all applicable statutes, rules and regulations to which they are subject; the descriptions of the results of such studies contained in the Registration Statement, General Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit to state a material fact necessary to make such statements not misleading; neither the Company nor any current Subsidiary has knowledge of any research studies not described in the Registration Statement, General Disclosure Package or the Prospectus the results of which reasonably call into question in any material respect the results of the research studies described in the Registration Statement, General Disclosure Package or the Prospectus; and neither the Company nor any current Subsidiary has received any written notices or correspondence from any foreign, state or local governmental body exercising authority or any institutional review board or comparable authority requiring or threatening the premature termination, suspension, material modification or clinical hold of any research studies conducted by or on behalf of, or sponsored by, the Company or any current Subsidiary or in which the Company or any current Subsidiary has participated that are described in the Registration Statement, General Disclosure Package or the Prospectus, and, to the Company’s knowledge, there are no reasonable grounds for the same. There has not been any violation of applicable law or regulation by the Company in its product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action, except where such violation could not, singly or in the aggregate, reasonab...
