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.
2.2. Laboratory will conduct the Study in accordance with the Protocol and/or Scope of Work, which may be amended from time to time upon the mutual agreement of Laboratory and Sponsor. If the amendment requires additional work on the part of the Laboratory, Laboratory will not conduct the additional work unless approved in writing in advance by Sponsor and if such approval is obtained, Laboratory will be paid an amount mutually agreed to by the parties. Laboratory agrees not to intentionally change or deviate from the Protocol without Sponsor’s prior approval. Laboratory may not make material deviations from the Protocol without the prior written approval of Sponsor. Deviations from the Protocol that are not material may be made in an emergency without Sponsor’s approval, provided that Laboratory shall use commercially reasonable efforts to obtain Sponsor’s verbal approval, which shall be subsequently confirmed by Sponsor in writing.
2.3. After the Study has been completed, Laboratory may be requested by Sponsor to provide additional consultation services concerning the Study performed by Laboratory. Upon such a request by Sponsor, Laboratory will provide the requested services and will be paid an amount mutually agreed to by the parties. These consultation services will be subject to the provisions on Confidentiality and Ownership set forth in Paragraphs 8 and 13, respectively.
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. 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.
3.2. It is a condition of the Award that the Institution has appropriate mechanisms in place for handling allegations of scientific misconduct. It is the responsibility of the Institution not Wellbeing of Women to investigate any such allegations.
3.3. The Institution shall ensure that:
a) The Funding is applied exclusively and appropriately in support of the Research Project and in accordance with the payment plan detailed in Schedule 3;
b) Sufficient resources are dedicated to support the Research Project;
c) All contractual requirements relating to the Research Project are met;
d) Researchers and staff performing the Research Project are appropriately qualified and supervised at all times.
3.4. The Institution must inform Wellbeing of Women without delay:
a) Of any change to the status of the Institution or the Award Holder which might affect their ability to perform the Research Project or to comply with this Agreement;
b) Of any significant alteration to the Research Project;
c) If the Award Holder leaves the Institution.
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. 4.1. The Recipient must:
4.1.1. carry out the Project in accordance with this Agreement and with all standard professional, scientific and ethical principles and standards;
4.1.2. comply with the Reporting Obligations;
4.1.3. enter into any third-party agreements as may be necessary to carry out the project; and
4.1.4. provide to the University, at its request, all reasonable information, documents and assistance relevant to the Project as may be necessary for the University to satisfy its obligations under the Program.
4.2. If the Grant includes funding to provide a scholarship to a student, the Recipient must:
4.2.1. appoint a student to conduct the Project;
4.2.2. supervise the carrying out of the Project by the student;
4.2.3. take all reasonable steps to ensure that the student carries out the Project in a competent and diligent manner, in accordance with this Agreement and with all standard professional, scientific and ethical principles and standards and national security classification information; and
4.2.4. provide the scholarship to the student from the Grant as specified in Schedule 1.
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. 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. 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 conduct the Research in accordance with the Protocol as approved by the UP Manila Ethics ...
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.
(b) Institute shall use commercially reasonable efforts to make available the resources necessary to conduct the Projects in accordance with the Research Plan including, without limitation, those set forth on Attachment B.
(c) The Institute has and will utilize for the conduct of the Projects under the Research Plan sufficient and qualified personnel, and appropriate facilities and equipment to perform the Research in a professional and competent manner, and will use commercially reasonable efforts to perform the Research under the Research Plan in a timely manner in accordance with such Research Plan and its timeline(s) and budget, and in accordance with all applicable federal and state statutes, and all applicable ordinances and regulations.
(d) Sponsor acknowledges that the Research contemplated under this Agreement will require funding from the United States Government. No funds from any corporate or commercial entity other than Sponsor will be used to fund any Project(s) subject to the Research Plan without the prior written consent of Sponsor. Other than as further approved in writing by Sponsor or as provided for herein below, Institute shall not accept or utilize funding from a third party other than the United States Government (“Third Party Funding”) or collaborate on the Research under a Research Plan with any third party other than the Xxxx Xxxxxxxxxx Cancer Research Center and its affiliated entities in a manner that would provide any third party ownership of or a license to any inventions first conceived or reduced to practice in the performance of a Research Plan under this Agreement (“Inventions”)...
Conduct of the Research. 4.1 The Recipient must:
4.1.1 appoint a Student to conduct the Project;
4.1.2 supervise the carrying out of the Project by the Student;
4.1.3 take all reasonable steps to ensure that the Student carries out the Project in a competent and diligent manner, in accordance with the Project Specification and with all reasonable professional, scientific and ethical principles and standards and national security classification information;
4.1.4 provide the Scholarship to the Student from the Grant as specified in Schedule 1;
4.1.5 enter into any third party agreements as may be necessary to carry out the project;
4.1.6 comply with the Reporting Obligations; and
4.1.7 provide to the University, at its reasonable request, all information, documents and assistance relevant to the Project as may be necessary for the University to satisfy its obligations under the DSDBI Grant Agreement and the DSI Participation Agreement.
Conduct of the Research. Promptly after the Effective Date and from time to time as necessary during the course of the Research Program, each Party will disclose to the other the Know-How and Patent Rights of such Party as the other Party reasonably needs to conduct its obligations and assigned tasks assigned in the Research Plan. Each Party shall conduct its activities assigned in the Research Plan in a good scientific manner, and in compliance in all material respects with the requirements of applicable laws and regulations and with applicable good laboratory practices and good manufacturing practices, to attempt to achieve its objectives efficiently and expeditiously. Each Party shall maintain laboratories, offices and all other facilities reasonably necessary to carry out the activities to be performed by such Party pursuant to the Research Plan. In conformity with standard pharmaceutical and biotechnology industry practices and the terms and conditions of this Agreement, each Party shall prepare and maintain, or shall cause to be prepared and maintained, complete and accurate written records, accounts, notes, reports and data with respect to activities conducted pursuant to the Research Program and, upon the other Party's written request, shall send legible copies of the aforesaid to the other Party. Upon reasonable advance notice, each Party agrees to make its employees and non-employee consultants reasonably available at their respective places of employment to consult with the other Party on issues arising during the Research Program and in connection with any request from any regulatory agency, including, without limitation, regulatory, scientific, technical and clinical testing issues.
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. Except as otherwise set forth in the Research Plan, Company will be solely responsible for conducting all Research Activities. Vertex shall 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 (including the Research Budget).
