The Research Project. 4.1. The Participants shall execute the Research Project in accordance with the Project Application, the Budget and the ICA.
4.2. The Research Project shall start on [… ] and shall end ultimately on […].
4.3. Any changes to the Project Application, the Budget or the ICA shall require prior written consent by the Management Board (as defined in the ICA) as well as Hartstichting.
The Research Project. 2.1 The University shall carry out its Project Responsibilities with reasonable skill and care, and in accordance with the timetable and scope set out specifically in the Project Plan (Schedule 2) in connection to The Patents which is the condition precedent of the Research Project.
2.2 At the end of each three month period, The University shall notify Somanta with a progress report on the Research Project setting out the following:-
2.2.1 the work which The University has carried out on the Research Project during the previous three months;
2.2.2 any data and/or results obtained during the previous three months;
2.2.3 the work that The University intends to carry out during the next three months; and
2.2.4 details of any inventions made in the course of carrying out the Research Project as described in the Project Plan.
2.3 Within 14 days of the end of each calendar quarter the parties shall meet to discuss progress on the Research Project in general and in particular The University’s latest progress report submitted under Clause 2.2. The University shall procure that the Project Scientists shall attend such meetings together with such other members of the University’s Project Team as Somanta may reasonably request. This meeting should occur at a destination and time previously agreed by both parties and at Somanta’s expense.
2.4 The University shall use The University’s Project Scientists to carry out and/or supervise The University’s Project Responsibilities. If, due to circumstances beyond the reasonable control of The University, it is necessary to replace any of the University’s Project Scientists then the parties shall promptly meet to discuss potential replacements of equivalent qualification and experience in the Field. The University shall not replace any of The University’s Project Scientists on the Research Project without the prior written approval of Somanta.
2.5 The University shall have discretion following consultation with Somanta to replace other members of The University’s Project Team during the Research Project with replacements of appropriate qualifications, skills and experience in the Field.
The Research Project. Cefic-LRI undertakes to sponsor the following Research Project: Pls. insert short description of the project. The details of the research project including the time line and milestones are described in Appendix 1 and summarised in the following table : Deliverables Milestones Timing The Research Institute agrees to carry out the Research Project as described in Appendix 1 and 2 and shall ensure that appropriate scientific staff shall be available. The Research Institute shall solely be responsible for the organisation of such co-operation and ensure that all deliverables and milestones are timely delivered. The Research Institute shall put in place necessary legal arrangements for this. This may include sub-contracting which shall not be deemed contrary to Article 5 of the present agreement. The Research Institute agrees to indemnify and hold harmless Cefic, its officers, directors, employees against all damages, liabilities or costs, including reasonable attorneys' fees and defence costs, to the extent caused by the Research Institute's negligent or wilful acts in the performance of the Research Project and the negligent or wilful acts of its subcontractors, except to the extent caused by negligence of Cefic. Notwithstanding anything to the contrary contained in this Agreement, the Research Institute’s total liability under this Agreement shall be limited to the total amount of remuneration pursuant to Article 3. The Research Institute shall publish at least one article related to the Research Project in the open access literature.
The Research Project. The parties will collaborate in the performance of the Research Project, pursuant to the following terms and conditions:
2.1. The Research Project shall include multiple trials as agreed upon by the Parties (the “Trials”), each Trial shall be performed in accordance with a Trial Protocol to be prepared by Rosetta for each Trial and agreed upon by THM (the “Protocol”). Each Protocol will be attached to this agreement as Appendix A1, A2 and so forth and constitute an integral part of this Agreement. The remuneration for each Trial shall be agreed upon by both Parties in advance and shall be specified in a budget schedule, executed by both Parties for each Trial and attached to the Trial’s Protocol (the “Budget Schedule”). The Budget Schedule of each Trial shall be attached to this agreement as Xxxxxxxx X0, X0 and so forth and constitute an integral part of this Agreement, the Protocol and the Budget Schedule collectively hereinafter: the “Protocol Plan”; The Protocol Plan for each Trial shall constitute an integral part of this Agreement.
2.2. The first Trial shall be conducted according to the Protocol attached to this Agreement as Appendix A1 and constituting an integral part thereof (“Protocol A1”). THM and Rosetta shall perform the activities mentioned in Protocol A1. THM shall perform the activities designated to it in Protocol A1 and in any other Protocol, directly or by employing the services of the Fund or any other third party to be agreed between THM and Rosetta (the entity who shall carry out the Trials on the part of THM: “the Research Entity”).
2.3. Rosetta shall oversee the conduct of the Research Project. THM shall designate a senior researcher currently contemplated to be Xxxx. Xxxxxx Rechavi (the “Investigator”) to collaborate with Rosetta in carrying out THM’s activities related to the Research Project.
2.4. A part of Rosetta’s activities under the Research Project shall be conducted in the facilities of the Hospital (“Rosetta’s Work”) by Rosetta’s employees and/or agents and/or representatives and/or contractor’s (“Rosetta’s Personnel”).
2.4.1. Rosetta’s Personnel shall be skillful, prudent, professionals and experienced in the field of the Research Project and shall hold any license and be qualified and authorized to perform Rosetta’s Work in accordance with the requirements of the applicable laws, regulations and guidelines.
2.4.2. Rosetta’s Work shall be performed by Rosetta’s Personnel in strict accordance with the Hospital’s and/or th...
The Research Project. 7.1 The manner in which, and the extent to which the Material may be used by the Recipient are as follows: The deidentified Material, obtained from [Collaborators’ institution] will be merged with the existing database from other contributing studies. The merged database will be used in the analysis to answer research questions; which will be predetermined by the core research group.
7.2 In the framework of this Agreement, the Parties may transfer Material to one another, which transfer shall be subject to the conditions of this Agreement. Parties shall list such Material also as Annexure to this Agreement and shall keep the Annexure up to date after each transfer of Material.
7.3 The Receiving Party shall utilise the Material solely for the conduct of the Project and shall in no case seek or have any person or corporate body seeking any commercial use of the Material or any other material that could not have been made but for the Material, unless explicitly agreed upon in this Agreement.
7.4 The Receiving Party shall not transmit by any means whatsoever all or part of the Material to any third party without the prior and written consent of the Disclosing Party.
7.5 The Receiving Party shall ensure that the importation, transport, use, maintenance and disposition of the Material will be conducted in strict accordance with and in compliance with all laws and regulations both local, nationally and internationally, including regulations for work with recombinant Material.
7.6 In the event where human tissue or products of human origin are implied by this Agreement, the Parties undertake to comply with the regulations related to human tissue or products of human origin, as enacted in the RSA Act on Human Tissue 65 of 1983, as amended and/or any other relevant act(s) and/or regulation(s) and in this regard to get the necessary approval from the Ethics Committee of either and/or both Parties, prior to the transfer of such human tissue or products of human origin.
The Research Project. 2.1 The parties respective obligations under this Agreement are conditioned upon the execution of the LICENSE AGREEMENTS by XXXXXXX.
2.2 After execution of the LICENSE AGREEMENTS, ONCOR, ONCORPHARM and XXXXXXX shall carry out the RESEARCH PROJECT in accordance with the RESEARCH PLAN attached hereto as Appendix A, which defines the primary responsibilities of each party. Appendix B sets forth details of the research staff at Xx. Xxxxxxxxx'x laboratory that shall be involved in the RESEARCH PROJECT. Appendix A and Appendix B shall be modified in good faith by the parties from time to time to accommodate changes in the RESEARCH PROJECT and the XXXXXXX employees and students participating in the RESEARCH PROJECT; provided, however, that such modifications to either Appendix A or Appendix B shall only become effective through a written amendment to this Agreement executed by all of the parties hereto.
2.3 ONCOR, ONCORPHARM and XXXXXXX shall allocate human resources to their respective responsibilities to EXECUTION COPY conduct the RESEARCH PROJECT substantially as set forth in the guidelines in the RESEARCH PLAN.
2.4 The parties shall use best efforts to carry out their respective responsibilities in the RESEARCH PROJECT. While the RESEARCH PLAN attached hereto as Appendix A is substantially controlling, it is understood that the parties shall cooperate and render research and clinical trials assistance to each other, including making their respective personnel available at reasonable times, in order to expedite carrying out the RESEARCH PROJECT efficiently and avoiding unwarranted duplication and e,xpenditure of effort.
2.5 The principal scientists or investigators who will direct the performance of the respective responsibilities of each party are, unless the parties otherwise agree, for XXXXXXX: Xx. Xxxx Xxxxxxxxx; for ONCOR: Xx. Xxxxxx
The Research Project. In order to make the most of your internship experience, you are required to complete a writing assignment that analyzes a political issue relevant to the work of your office. Final writing projects should be 8-20 pages (depending on units, see below) and should be based on substantial scholarly research, including consideration of the relevant literature. The focus should be on a specific policy or issue related to your internship. Please discuss your project in detail with the Internship Coordinator to tailor the assignment to your interests.
A) Project part 1 – Topic & Research Methods: due Wednesday, June 5, by 5:00 p.m. (PST) This assignment must be 2 pages in length describing the topic(s) for your analytic essay and how you plan on going about your research. There are four specific components of the assignment, i.e.,
(1) research question, (2) statement of methodology, (3) 2 to 4 paragraphs on how you see the paper unfolding, and (4) at the top of page 3, a preliminary bibliography with at least 3 properly formatted sources (use MLA format).
B) Project part 2 – Outline & Bibliography: due Wednesday, July 10 by 5:00 p.m. (PST) This assignment must be a 3 to 5 page summary and detailed outline of some of the research you have done for your paper. Please use traditional outline form, e.g., I, a, i, 1. You will also need to
C) Final Paper/Project: due Tuesday, August 6th, by 5:00 p.m. (PST)
The Research Project. Proposal Summary: During mechanical interaction with our environment, we derive a perceptual experience which may be compared to the experience that results from acoustic and optic stimulation. Progress has been made towards the discovery of mechanisms subserving the conscious experience of interacting with mechanical objects. This progress is due in part to the availability of new instruments that can tightly control mechanical stimulation of both the ascending, i.e. sensory, and descending, Specific Aims
1. slip,
2. intra-contact deformation patterns, 3. contact velocity, 4. local deformation, 5. motoric activity, and
The Research Project. 2.1 Cefic-LRI undertakes to sponsor the following Research Project: The details of the Research Project including the time line and milestones are described in Appendix 1 and summarised in the following table:
2.2 The Research Institute agrees to carry out the Research Project as described in Appendices 1 & 2. As described in both appendices this Research Project is conducted by way of co-operation between different research bodies.
2.3 The Research Institute shall solely be responsible for the organisation of such co- operation and ensure that all deliverables and milestones are timely delivered. The Research Institute shall put in place necessary legal arrangements for this. This may include sub-contracting which shall not be deemed contrary to Article 5 of the present agreement.
2.4 Under no circumstances shall Cefic be liable for any damages arising directly or indirectly from such co-operation and the Research Institute shall assume all liabilities.
The Research Project. 4.1 In accordance with the principles of freedom and independence of research, the Recipient shall be free to choose the topic within macroeconomics with emphasis on monetary and financial stability issues and to conduct the Research Project in cooperation with the Host Institution.
4.2 Any material re‐definition of the topic, or other material changes or developments to the Research Project in cooperation with the Host Institution, which may affect the scope and purpose of the Scholarship, shall be reported to and accepted by the Committee in advance.
4.3 Upon finalization of the Research Project, the Recipient shall inform the Committee and provide to the Committee two printed copies and an electronic copy of the final thesis or articles submitted for the PhD degree.
