Management of the Research Program Sample Clauses

Management of the Research Program. (a) The Research Collaboration will be managed by a Joint Research Committee composed of 4 members: 2 members to be designated by each party. The initial composition of the Joint Research Committee is set forth in Exhibit C. Each party will be entitled to designate from time-to-time a successor to the member previously designated by it unless the other party has a reasonable objection to such successor. (b) The Joint Research Committee will hold meetings as necessary but at least twice per year, at times and locations to be mutually agreed upon. The minutes of the meetings will be recorded and marked "confidential" and will be subject to the secrecy obligations and restrictions on use contained in Paragraphs 12.2 and 12.3. * CONFIDENTIAL TREATMENT REQUESTED (c) The Joint Research Committee will review and evaluate the work on the Research Collaboration. Its functions will be to decide: (i) on Targets to be included within the Research Collaboration; (ii) on Research Target Profiles for any Target (including any subsequent modifications of such Research Target Profile); (iii) on therapeutic indications to be pursued for Compounds inhibiting a Target; (iv) the territorial patenting strategy for Compounds and the "freedom to operate" position by patent due diligence on new Targets or Compounds; (v) assignment of financial resources and personnel to specific Targets; and/or emphasis among Targets; (vi) approval of Target-specific Research Plans; (vii) determination of whether a Compound fulfills the Research Target Profile; (viii) approval of Excess Research Costs; (ix) when necessary, on taking appropriate action to adopt alternative approaches or to make recommendations on redirecting or restructuring the Research Plan set out in Exhibit B; and (x) determine the detailed manufacturing specifications for research Compounds (d) The Joint Research Committee will act by unanimous decision. Disputes will be resolved pursuant to Paragraph 13.11 hereof.
Management of the Research Program. The Parties will establish and maintain a joint steering committee to oversee the conduct of the Research Program and, following completion of the Research Program, to serve as an information-sharing forum with respect to development, registration, Manufacture and commercialization of Lead Compounds and Products by or on behalf of AstraZeneca, its Affiliates and Sublicensees pursuant to this Agreement (the “JSC”). The JSC will be established, operated and governed in accordance with the policies and procedures set forth in APPENDIX 2 attached hereto (the “Research Program Management Charter”). The Research Program Management Charter may only be amended by mutual written agreement of the Parties. As needed, the JSC will establish subcommittees and working groups that will report to the JSC to further the objectives of the Research Program and, following completion of the Research Program, to further the objectives of the information-sharing objectives of the JSC.
Management of the Research Program. (a) The Research Collaboration will be managed by a Joint Research Committee composed of 4 members: 2 members to be designated by each party. The initial composition of the Joint Research Committee is set forth in Exhibit C. Each party will be entitled to designate from time-to-time a successor to the member previously designated by it unless the other party has a reasonable objection to such successor. (b) The Joint Research Committee will hold meetings as necessary but at least twice per year, at times and locations to be mutually agreed upon. The minutes of the meetings will be recorded and marked "confidential" and will be subject to the secrecy obligations and restrictions on use contained in Paragraphs 12.2 and 12. (c) The Joint Research Committee will review and evaluate the work on the Research Collaboration. Its functions will be to decide: (i) on Targets to be included within the Research Collaboration; * CONFIDENTIAL TREATMENT REQUESTED 6 (ii) on Research Target Profiles for any Target (including any subsequent modifications of such Research Target Profile);
Management of the Research Program. 5.1 Research Management Committee. -----------------------------
Management of the Research Program. The JMT shall establish and may amend the scientific objectives of the Research Program from time to time and shall review the progress
Management of the Research Program. 3.1 Steering Committee. Benitec and 4D Molecular hereby establish a Steering Committee to: a. oversee the collaboration between the Parties; b. review and evaluate the Research Program’s progress; c. recommend to the Parties any amendments to revise or add studies to the Research Plan, for the Parties’ written approval and adoption if they are in agreement, according to Section 2.3; d. coordinate the publication of the Research Program’s results; e. monitor the exchange of information and materials between the Parties; f. disclose to the other Party advances, new developments, and discoveries related to the Parties’ activities under this Agreement and the Research Plan; and g. review and discuss AAV Capsid Variants proposed for selection and advancement to validation studies under the Research Program. h. discuss and review the funding to the program, including management of records thereof. i. discuss and approve budgets for the research program, as well as payments.
Management of the Research Program 

Related to Management of the Research Program

  • Research Program The term “

  • Development Program A. Development activities to be undertaken (Please break activities into subunits with the date of completion of major milestones) B. Estimated total development time

  • Development of the Project 4.1 TSP's obligations in development of the Project: a. for procuring and maintaining in full force and effect all Consents, Clearances and Permits, required in accordance with Law for development of the Project; b. for financing, constructing, owning and commissioning each of the Element of the Project for the scope of work set out in Schedule 1 of this Agreement in accordance with: i. the Electricity Act and the Rules made thereof; ii. the Grid Code; iii. the CEA Regulations applicable, and as amended from time to time, for Transmission Lines and sub-stations: • the Central Electricity Authority (Technical Standards for Connectivity to the Grid) Regulations, 2007; • Central Electricity Authority (Technical Standards for construction of Electrical Plants and Electric Lines) Regulation, 2010; • Central Electricity Authority (Grid Standard) Regulations, 2010; • Central Electricity Authority (Safety requirements for construction, operation and maintenance of Electrical Plants and Electrical Lines) Regulation, 2011; • Central Electricity Authority (Measures relating to Safety and Electricity Supply) Regulation, 2010; • Central Electricity Authority (Technical Standards for Communication System in Power System Operation) Regulations, 2020. iv. Safety/ security Guidelines laid down by the Government; v. Prudent Utility Practices, relevant Indian Standards and the Law; not later than the Scheduled COD as per Schedule 2 of this Agreement; c. for entering into a Connection Agreement with the concerned parties in accordance with the Grid Code. d. for owning the Project throughout the term of this Agreement free and clear of any encumbrances except those expressly permitted under Article 15 of this Agreement; e. to co-ordinate and liaise with concerned agencies and provide on a timely basis relevant information with regard to the specifications of the Project that may be required for interconnecting the Project with the Interconnection Facilities; f. for providing all assistance to the Arbitrators as they may require for the performance of their duties and responsibilities; g. to provide to the Nodal Agency and CEA, on a monthly basis, progress reports with regard to the Project and its execution (in accordance with prescribed form) to enable the CEA to monitor and co-ordinate the development of the Project matching with the Interconnection Facilities; h. to comply with Ministry of Power order no. 25-11/6/2018 – PG dated 02.07.2020 as well as other Guidelines issued by Govt. of India pertaining to this; i. to procure the products associated with the Transmission System as per provisions of Public Procurement (Preference to Make in India) orders issued by Ministry of Power vide orders No. 11/5/2018 - Coord. dated 28.07.2020 for transmission sector, as amended from time to time read with Department for Promotion of Industry and Internal Trade (DPIIT) orders in this regard (Procuring Entity as defined in above orders shall deemed to have included Selected Bidder and/ or TSP). Also, to comply with Department of Expenditure, Ministry of Finance vide Order (Public Procurement No 1) bearing File No. 6/18/2019- PPD dated 23.07.2020, Order (Public Procurement No 2) bearing File No. 6/18/2019-PPD dated 23.07.2020 and Order (Public Procurement No. 3) bearing File No. 6/18/2019-PPD, dated 24.07.2020, as amended from time to time, regarding public procurement from a bidder of a country, which shares land border with India; j. to submit to Nodal Agency information in the prescribed format [To be devised by Nodal Agency] for ensuring compliance to Article 4.1 i) above. k. to comply with all its obligations undertaken in this Agreement. 4.2 Roles of the Nodal Agency in implementation of the Project: 4.2.1 Subject to the terms and conditions of this Agreement, the Nodal Agency shall be the holder and administrator of this Agreement and shall inter alia: a. appoint an Independent Engineer within 90 days of the Effective Date b. provide letters of recommendation to the concerned Indian Governmental Instrumentality, as may be requested by the TSP from time to time, for obtaining the Consents, Clearances and Permits required for the Project; c. coordinate among TSP and upstream/downstream entities in respect of Interconnection Facilities; and d. monitor the implementation of the Agreement and take appropriate action for breach thereof including revocation of guarantees, cancellation of Agreement, blacklisting etc e. provide all assistance to the Arbitrators as required for the performance of their duties and responsibilities; and f. perform any other responsibility (ies) as specified in this Agreement.

  • Collaboration activities 4.1 The Collaboration Suppliers will perform the Collaboration Activities and all other obligations of this Agreement in accordance with the Detailed Collaboration Plan. 4.2 The Collaboration Suppliers will provide all additional cooperation and assistance as is reasonably required by the Buyer to ensure the continuous delivery of the services under the Call-Off Contract. 4.3 The Collaboration Suppliers will ensure that their respective subcontractors provide all cooperation and assistance as set out in the Detailed Collaboration Plan.

  • Collaboration 31.1 If the Buyer has specified in the Order Form that it requires the Supplier to enter into a Collaboration Agreement, the Supplier must give the Buyer an executed Collaboration Agreement before the Start date. 31.2 In addition to any obligations under the Collaboration Agreement, the Supplier must: 31.2.1 work proactively and in good faith with each of the Buyer’s contractors 31.2.2 co-operate and share information with the Buyer’s contractors to enable the efficient operation of the Buyer’s ICT services and G-Cloud Services