Conduct of the Research. 2.1. Laboratory will maintain industry standards of professional conduct in the performance of the Study and in the preparation of all reports. Laboratory will adhere to all government laws and regulations applicable to the conduct of the Study. If applicable, and as set forth in the Protocol and/or Scope of Work, Laboratory will perform the Study in compliance with the current laboratory practices of the appropriate governmental regulatory agency(ies). * Confidential Treatment Requested by the Registrant. Redacted Portion Filed Separately with the Commission.
Conduct of the Research. 4.1. The Recipient must:
Conduct of the Research. The Project Proposal shall set forth the work to be performed by the University relating to the Research. The University shall perform its work consistent with the Project Proposal and the terms of this Agreement. University shall complete the Project Proposal prior to the expiration date as specified therein.
Conduct of the Research. Each Party, directly or through its Affiliates or permitted Subcontractors, will use Commercially Reasonable Efforts to conduct the activities allocated to it in the Research Plan in accordance with the Research Plan, including the timelines set forth therein, and in a professional and timely manner. Each Party will, and will require its Affiliates and Subcontractors to, perform its obligations under the Research Plan in compliance with Applicable Law. [***]. Vertex will reimburse Company in accordance with Section 5.8 for Company’s FTE Costs and Out-of-Pocket Costs incurred in conducting such Research Activities in accordance with the Research Plan and Research Budget.
Conduct of the Research. 3.1. The Institution must inform Xxxxxxxxx of Women in writing of the Commencement Date. If the Research Project has not started within 6 months of the date of this Agreement, Wellbeing of Women may terminate this Agreement by giving the Institution notice in writing and without further liability or obligation to the Institution.
Conduct of the Research. The parties agree to conduct the Research based upon the terms and conditions contained in this Agreement and in accordance with the Protocol attached as Appendix A. Site Evaluation. the UNIVERSITY will conduct an evaluation of the planned facilities to be used by the Institution for the Research before the performance of the Research and before implementation of the Research. Principal Investigators. DR. __________________________, MD Department of _____, [Name of Hospital] DR. __________________________, MD Department of _____, [Name of Hospital] Responsibilities of the UNIVERSITY. To provide the Institution with the necessary background information needed for the appropriate and safe conduct of the Research; To ensure that the Investigator/s are familiar with the details of the Protocol and other liabilities and responsibilities defined in this agreement, and that Investigators are committed to act accordingly; To ensure necessary training and orientation of the personnel of the Institution involved in the Research in order to conduct the Research in accordance with the Protocol; To provide the Institution with the data and documents needed for conducting the Research and guaranteeing the safety of the participants. The data and documents provided by the UNIVERSITY may be used solely for the conduct of this Research in accordance with this agreement. Responsibilities of the Institution To ensure that qualified and instructed personnel and adequate equipment are available for the Research and that the Research may also in other respects be conducted in safe conditions; To allow participation of the involved research personnel conducting the Research in meetings and other education arranged by the UNIVERSITY; To allow monitoring and auditing at the Research site to be conducted by the UNIVERSITY, as well as domestic and foreign regulatory authorities, and, if necessary, to assist in the executing thereof. To provide the logbook of patients to the research assistant for participant selection; To provide pass or identification card for research assistant. Responsibilities of the Principal Investigator To be fully acquainted with the Protocol and all information and documents provided by the UNIVERSITY concerning the conduct of the clinical Research; To ensure that qualified and instructed personnel, as well as adequate equipment are available for the Research, and that the Research can also in all other respects be conducted under safe conditions; To conduc...
Conduct of the Research. (a) The Research activities shall be carried out in accordance with a written research plan, timeline and budget (“Research Plan”), as may be amended from time-to-time, to be prepared and approved by the Committee. The Research Plan shall detail the objectives of the applicable Project(s), and for each Project to be conducted in connection with the Research: activities to be performed, resources that will be utilized (staffing, facilities, capital equipment, etc.), deliverables, budgets and associated timelines for the foregoing. If the Committee is unable to prepare a Research Plan that is reasonably acceptable to both of Institute and Sponsor, [***]. Institute and Sponsor will each use commercially reasonable efforts to carry out their respective research and development activities as promptly as practicable in accordance with the Research Plan.
Conduct of the Research. (a) The Research will be managed and directed by the JRC, as discussed in Article 4 hereof. The JRC will coordinate the Research effort of the Parties, expedite the progress of work being done under the Research Plan and prevent duplication of efforts.
Conduct of the Research. Project[;Limited Right to Subcontract Project Activities][INCLUDE AS NECESSARY].
Conduct of the Research. A. Principal Investigator - The Research Program will be supervised by [ * ] of CSHL, as Principal Investigator. If, for any reason, he is unable or unwilling to continue to serve as Principal Investigator, CSHL and Sponsor shall use their reasonable best efforts to locate a suitable successor as Principal Investigator to continue the Research Program, or select alternative research work. If the parties cannot mutually agree on a successor or alternative research work, and if Sponsor elects not to terminate the License Agreement as provided in Section VII.B(3) of the License Agreement, then future funding provided for under Section 4.A hereof shall be reduced by [ * ] commencing on the date [ * ] becomes unable or unwilling to serve as Principal Investigator, and Sponsor shall continue to pay to CSHL such reduced amount as [ * ]. The schedule of reduced funding payments shall continue to be in accordance with Section 5 hereof. The scientific contact to the Research Program from the Company will be [ * ].
