Joint Project Team Responsibilities Sample Clauses

Joint Project Team Responsibilities. The Joint Project Team shall be responsible, with the oversight and approval of the JSC, for formulating and executing the specific details of the Parties' Development collaboration, including, without limitation, preparing for and executing the Development activities contemplated hereunder. The Joint Project Team shall prepare the Development Plan and each associated Annual Work Plan/Budget in accordance with Section 4.2. Except as set forth in Section 4.7, the Joint Project Team shall also have the responsibility of selecting the criteria for Development of Antegren or, as applicable, other Licensed Product; making decisions regarding the design and implementation of all research programs; selecting and designing clinical trials for all proposed indications; developing a publication and scientific symposia strategy and a calendar of key scientific and clinical meetings; conducting market research and development activities prior to formation of Joint Commercialization Team; devising the content of and filing strategy for all Clinical Trial Applications and Drug Approval Applications; through the representatives on the Joint Project Team with regulatory expertise, coordinating interactions with Regulatory Authorities and, along with the Joint Commercialization Team, developing and implementing standard operating procedures for adverse event reporting and compliance with other regulatory requirements in the Territory, consistent with Article 13; through the Joint Patent Committee, coordinating patent and trademark-related activities, subject to Section 3.4; and implementing other activities necessary to the successful completion of the collaboration and for exchanging information and facilitating cooperation and coordination between the Parties as they exercise their respective rights and meet their respective obligations under this Agreement. In addition to such other reports as required by the JSC, the Joint Project Team shall submit to the JSC its written determinations of all Commercially Significant Indications for Antegren or, as applicable, other Licensed Product, as such determinations are made, and a determination of its recommendations as to the priority among such indications and the priority among the countries within the Territory in which the Joint Project Team expects to seek Regulatory Approval of Antegren, or, as required, other Licensed Product. The Joint Project Team will be responsible for all other activities assigned to it by the JSC.
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Joint Project Team Responsibilities. The JPT’s primary responsibilities shall include, but shall not be limited to, the following functions or roles:
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Joint Project Team Responsibilities. The JPT’s primary responsibilities shall include, but shall not be limited to, the following functions or roles: • Serving as technical lead and principal point of contact for all matters set forth in the Schedules; • Overseeing project planning and progress and coordinating all activities set forth in the Schedules; • Recommending updates to the Schedules including tactics and risk mitigation to the JSC; • Leading meetings (at least monthly) to facilitate review and coordinated interpretation of data, information sharing, and timeline monitoring; Confidential and Proprietary Information of Tokai and QIAGEN • Facilitating issue resolution at the Team level and escalating issues to the JSC; and • Coordinating with the Alliance Managers to provide input to the agenda, preparing thoroughly for meetings, attending meetings and ensuring follow up on action items.
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Joint Project Team Responsibilities. (i) The Joint Project Team shall be responsible for formulating overall development plans and an annual development budget, for making overall decisions regarding the priority and design of all clinical trials for new indications (except for Registry Studies and ISTs, defined below), for recommending to the JSC which Party will be responsible for implementing clinical studies for each indication (other than Registry Studies), for developing a publication strategy and a calendar of key scientific and clinical meetings and other events for Licensed Product, for exchanging information and facilitating cooperation and coordination between the Parties as they exercise their respective rights and meet their respective obligations under this Agreement, for determining the priority with respect to seeking Regulatory Approval of Licensed Product, for approving third party manufacturing and supply agreements, for recommending to the JSC or the GDC (via the OSI-774 Liaison Team, in the case of the GDC), as the case might be, new Lifecycle Initiatives hereunder, and for implementing all activities approved by the JSC or the GDC, as the case might be.
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Joint Project Team Responsibilities. The Joint Project Team shall be responsible for formulating overall development plans and an annual budget, for making overall decisions regarding the priority and design of all clinical trials for new indications, for determining which Party will be responsible for implementing clinical studies for each indication, for developing a publication strategy and a calendar of key scientific and clinical meetings and other events for Licensed Products, for exchanging information and facilitating cooperation and coordination between the Parties as they exercise their respective rights and meet their respective obligations under this Agreement, for determining the priority with respect to seeking Regulatory Approval of Licensed Products, for approving third party manufacturing and supply agreements, and for implementing all activities approved by the JSC. In addition, the Joint Project Team may designate subteams as appropriate to facilitate coordination and cooperation in key areas. Specifically, the Joint Project Team will designate a Joint Regulatory Subteam to coordinate efforts as may be necessary for NDA filing and other regulatory activities. The Joint Project Team will prepare a draft Development Budget/Plan, and draft annual development and joint marketing and sales budgets, as applicable, by August 15 of the then-current calendar year, and a final Development Budget/Plan, for JSC approval, by September 15 of the then-current calendar year. In addition, the Joint Project Team Leaders will participate in the OSI-774 Liaison Team, described in Section 3.4 below, to exchange information, and facilitate cooperation and coordination, between the Parties and Roche, pursuant to the Tripartite Agreement.
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Joint Project Team Responsibilities. The Joint Project Team shall be responsible for:
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Joint Project Team Responsibilities. Each Joint Project Team will oversee and be responsible for all development activities for its Licensed Product in the Field of Use in the Territory as set forth in the Development and Commercialization Plan. Such responsibilities shall include:
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Related to Joint Project Team Responsibilities

  • Development Responsibilities Unless the Parties agree in writing upon an alternate allocation of responsibility, the Parties shall have the following rights and obligations with respect to operational responsibilities under each Development Plan:

  • Joint Responsibilities 2.1.1 University and Affiliate each will identify, and notify each other of, a person responsible for serving as its liaison during the course of this affiliation. The appointment of liaisons shall be subject to mutual approval of the parties.

  • ALPS’ Responsibilities In connection with its performance of TA Web, ALPS shall:

  • Specific Responsibilities In addition to its overall responsibility for monitoring and providing a forum to discuss and coordinate the Parties’ activities under this Agreement, the JSC shall in particular:

  • Client Responsibilities You are responsible for (a) assessing each participants’ suitability for the Training, (b) enrollment in the appropriate course(s) and (c) your participants’ attendance at scheduled courses.

  • Contractor Responsibilities 19.1. Contractor shall perform national criminal history checks for Ohio, Indiana, and Kentucky, and 10-panel drug screening tests on all prospective employees performing work under this RFP or coming onto a CMHA property and any resulting contract and provide summaries of the results to the Authority if requested. For the purposes of this section, the term “employees” includes contractor. Prospective employees whose criminal background check discloses a misdemeanor or felony involving crimes of moral turpitude, sexual offenses or harm to persons or property shall not be employed to perform work under this RFP or any resulting contract. Contractor is required to perform drug screening of all employees and to ensure acceptable test results. Criminal history and drug screening checks will be completed at the sole expense of the contractor. Any employee of the Contractor suspected of being under the influence of drugs and or alcohol will be reported to the appropriate personnel at CMHA and/or other local law enforcement. If the employee is determined to be under the influence of drugs or alcohol in any form or manner, or believed by proper authority to be dealing in illicit sale of alcohol or drugs they will be removed and shall not be allowed to return to any job site on the Authority’s property. The Contractor’s contract may be suspended and/or terminated should such a situation occur or if the Contractor fails to submit results pursuant to this section.

  • Joint Responsibility If the Seller determines that the Interface Problem is attributable partially to the design of a Warranted Part and partially to the design of any Supplier Part, the Seller will, if so requested by the Buyer, seek a solution to the Interface Problem through cooperative efforts of the Seller and any Supplier involved. The Seller will promptly advise the Buyer of such corrective action as may be proposed by the Seller and any such Supplier. Such proposal will be consistent with any then existing obligations of the Seller hereunder and of any such Supplier towards the Buyer. Such corrective action, unless reasonably rejected by the Buyer, will constitute full satisfaction of any claim the Buyer may have against either the Seller or any such Supplier with respect to such Interface Problem.

  • Monitoring Responsibilities The Custodian shall furnish annually to the Fund, during the month of June, information concerning the foreign sub-custodians employed by the Custodian. Such information shall be similar in kind and scope to that furnished to the Fund in connection with the initial approval of this Contract. In addition, the Custodian will promptly inform the Fund in the event that the Custodian learns of a material adverse change in the financial condition of a foreign sub-custodian or any material loss of the assets of the Fund or in the case of any foreign sub-custodian not the subject of an exemptive order from the Securities and Exchange Commission is notified by such foreign sub-custodian that there appears to be a substantial likelihood that its shareholders' equity will decline below $200 million (U.S. dollars or the equivalent thereof) or that its shareholders' equity has declined below $200 million (in each case computed in accordance with generally accepted U.S. accounting principles).

  • Owners Responsibilities 2.1. The Owner shall designate in writing a project coordinator to act as OWNER's representative with respect to the services to be rendered under this Agreement (hereinafter referred to as the "Project Coordinator"). The Project Coordinator shall have authority to transmit instructions, receive information, interpret and define OWNER's policies and decisions with respect to CONTRACTOR's services for the Project. However, the Project Coordinator is not authorized to issue any verbal or written orders or instructions to the CONTRACTOR that would have the effect, or be interpreted to have the effect, of modifying or changing in any way whatever:

  • Customer Responsibilities Customer shall:

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