Supply Team Sample Clauses

Supply Team. Within thirty (30) days after the Effective Date, Schering and Indevus will establish a team consisting of four (4) members, two (2) representatives nominated by Schering and two (2) representatives by Indevus, which team shall discuss and supervise all issues in the Manufacturing and supply of Product (“Supply Team”). Unless otherwise agreed between the Parties, the Supply Team will meet quarterly (in person, telephonically or via videoconference). Either Party may replace any or all of its representatives in and/or invite other representatives of such Party to attend meetings of the Supply Team at any time upon written notice to the other Party. Regardless of the number of individuals attending any Supply Team meeting, Schering and Indevus shall have a single vote each.
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Supply Team. Each party will forthwith upon execution of this Agreement establish a Supply Team, with each party appointing two of its employees to be members of the Supply Team. The members from each party collectively will have one (1) vote. Each party may replace any or all of its representatives on the Supply Team at any time upon written notice to the other party.
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Supply Team. The Parties shall establish a supply team, or ST, pursuant to the provisions of the Supply Agreement.
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Supply Team. The Parties will form a team (the “Supply Team”) to oversee the activities contemplated by this Manufacturing Agreement. The Supply Team will be comprised of members appointed by Lilly and members appointed by ViroPharma. ViroPharma and Lilly will each appoint one of its members as that Party’s lead and that individual will be the contact person for the other Party and will serve as the manufacturing representative and member of the Implementation Team referred to in Section 13.1 of the Assignment Agreement. The Supply Team may meet as reasonably needed and determined by the Supply Team as appropriate to conduct business, oversee the Marketed Product supply process and assure a smooth transition to the Third Person Supply Chain or any other third party manufacturer designated by ViroPharma.
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Supply Team. The Parties hereby establish a Supply Team to perform the functions described in or referred to herein. The Supply Team is intended to facilitate decision-making and management of the Parties’ activities under this Agreement, and each Party agrees to use good faith and cooperative efforts to facilitate and assist the efforts of the Supply Team. The Supply Team will (i) oversee and monitor the timely supply of API and Components and the production of Bulk and Finished Product to ensure forecasted Delivery Dates are met; (ii) make recommendations to the Parties with respect to key written performance [***] Certain information in this document has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions. metrics with respect to the production of Bulk and Finished Product including yields, quality parameters, and timely delivery; (iii) evaluate and, as appropriate, recommend [***] changes and other improvements; (iv) monitor and report each Party’s achievement of performance efficiencies and related metrics; (v) coordinate the activities of the Parties in support of RELYPSA’s NDA submission and the PAI, and ensure the timely exchange of information, documents and other support of these efforts by the Parties, (vi) assist with the handling of complaints, adverse events, recalls, and return processes in accordance with Article 10 and the applicable procedures in the Quality Agreement; and (vii) provide such other related functions as the Parties shall mutually agree from time to time.
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Supply Team. The Parties will form a team (the “Supply Team”) to oversee the activities contemplated by this Manufacturing Agreement. The Supply Team will be comprised of members appointed by Lilly and members appointed by Advancis. Advancis and Lilly will each appoint one of its members as that Party’s lead and that individual will be the contact person for the other Party. During the first ninety (90) days after the Effective Date, the Supply Team may meet as reasonably needed and determined by the Supply Team as reasonably appropriate to conduct business and assure a smooth transition.
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Supply Team. The Parties hereby establish a Supply Team to perform the functions described in or referred to herein. The Supply Team is intended to facilitate decision-making and management of the Parties’ activities under this Agreement, and each Party agrees to use good faith and cooperative efforts to facilitate and assist the efforts of the Supply Team. The Supply Team will (i) oversee and monitor the timely supply of API and Components and the production of Bulk and Finished Product to ensure forecasted Delivery Dates are met; (ii) make recommendations to the Parties with respect to key written performance metrics with respect to the production of Bulk and Finished Product including yields, quality parameters, and timely delivery; (iii) evaluate and, as appropriate, recommend [***] changes and other improvements; (iv) monitor and report each Party’s achievement of performance efficiencies and related metrics; (v) coordinate the activities of the Parties in support of RELYPSA’s NDA submission and the PAI, and ensure the timely exchange of information, documents and other support of these efforts by the Parties, (vi) assist with the handling of complaints, adverse events, recalls, and return processes in accordance with Article 10 and the applicable procedures in the Quality Agreement; and (vii) provide such other related functions as the Parties shall mutually agree from time to time.
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Supply Team. To facilitate an orderly transition of the Activities from Lilly to NEOSAN, the Parties will form a team (the "Supply Team") to oversee the activities contemplated by this Manufacturing Agreement. The Supply Team will be comprised of members appointed by Lilly and members appointed by NEOSAN. NEOSAN and Lilly will each appoint one of its members as that Party's lead and that individual will be the contact person for the other Party. During the first ninety (90) days after the Closing Date, the Supply Team may meet as reasonably needed and determined by the Supply Team as reasonably appropriate to conduct business and assure a smooth transition.
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Supply Team 
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Related to Supply Team

  • Joint Manufacturing Committee In accordance with Section 2.5(c)(iv), the Parties shall promptly establish and convene a joint Manufacturing Committee (the “JMC”) for the overall coordination and oversight of the Manufacturing of clinical and commercial supplies of the Product under this Agreement as provided in the Manufacturing Plan (including the Manufacture of API, Drug Product and Finished Product). The JMC shall consist of representatives of each Party, and shall operate by procedures, as set forth in Section 2.5. The role of the JMC shall be:

  • Project Team To accomplish Owner’s objectives, Owner intends to employ a team concept in connection with the construction of the Project. The basic roles and general responsibilities of team members are set forth in general terms below but are more fully set forth in the Design Professional Contract with respect to the Design Professional, in the Program Management Agreement with any Program Manager, and in this Contract with respect to the Contractor.

  • Steering Committee The Project Manager shall set up a Steering Committee for the Project, consisting of representatives from the Department, the Contractor, and any other key organisations whom the project will impact on, to be agreed between the parties. The function of the Steering Committee shall be to review the scope and direction of the Project against its aims and objectives, monitor progress and efficiency, and assess, manage and review expected impact and use of the findings from the Project. The Committee shall meet at times and dates agreed by the parties, or in the absence of agreement, specified by the Department. The Contractor’s representatives on the Steering Committee shall report their views on the progress of the Project to the Steering Committee in writing if requested by the Department. The Contractor’s representatives on the Steering Committee shall attend all meetings of the Steering Committee unless otherwise agreed by the Department.

  • Joint Project Team As soon as possible after the Effective Date, the Parties shall establish a joint project team (the “JPT”) which shall be initially responsible for the day-to-day operations of the Initial Target Program. The JPT shall also be responsible for the day-to-day operations of all other Collaboration Programs when they become ***Portions of this page have been omitted pursuant to a request for Confidential Treatment and filed separately with the Commission. effective; provided, that if multiple JPTs are needed due to different Targets or disease areas, then the Parties may establish separate JPTs for different Collaboration Programs. The JPT shall be comprised of representatives from each of GSK and Adaptimmune with the appropriate scientific expertise with respect to the conduct of the Development Plans (and such representatives may vary depending on the relevant Project Phase) and shall meet on a monthly basis (or more or less frequently as agreed by the Parties) at Adaptimmune’s facilities, GSK’s facilities or via teleconference at such times as may be agreed by the Parties during the term of the applicable Collaboration Program. The JPT will report to the JSC and will be responsible for the day-to-day management of the conduct of the Development Plans including any non-material changes to the Development Plans, overseeing the conduct of experiments and reviewing data resulting from such experiments as set forth in the Development Plans, proposing amendments to the Development Plans, proposing new Development Plans to the JSC for new Collaboration Programs for JSC approval, discussing potential Lead Candidates and Development Candidates for proposal to the JSC. All decisions of the JPT on matters for which it has responsibility shall be made unanimously. In the event that the JPT is unable to reach a unanimous decision within ten (10) Business Days after it has met and attempted to reach such decision, then either Party may, by written notice to the other, have such issue submitted to the JSC for resolution in accordance with Section 4.5. Each Party will bear all expenses it incurs in regard to participating in all meetings of the JPT, including all travel and living expenses. Each JPT shall automatically cease to exist on completion of the relevant Collaboration Programs that it supports and exercise or expiry of all Collaboration Program Options applicable to such Collaboration Programs.

  • Joint Steering Committee [***] following the Effective Date [***], a joint steering committee (the “JSC”) will be established by the Parties to provide oversight and to facilitate information sharing between the Parties with respect to the activities under this Agreement.

  • Research Committee 2.2.1 Establishment and Functions of RC. ---------------------------------

  • Project Managers The JBE’s project manager is: [Insert name]. The JBE may change its project manager at any time upon notice to Contractor without need for an amendment to this Agreement. Contractor’s project manager is: [Insert name]. Subject to written approval by the JBE, Contractor may change its project manager without need for an amendment to this Agreement.

  • Project Leaders Within [**] Business Days after the Effective Date, each Party will appoint (and provide written notice to the other Party of the identity of) a senior representative having a general understanding of biopharmaceutical discovery and development issues to act as its project leader under this Agreement (each, a “Project Leader”). The Project Leaders will serve as the contact point between the Parties with respect to the Research Program, and will be primarily responsible for: (a) facilitating the flow of information and otherwise promoting communication, coordination of the day-to-day work and collaboration between the Parties; (b) providing single point communication for seeking consensus internally within the respective Party’s organization; and (c) raising cross-Party or cross-functional disputes in a timely manner. The Project Leaders shall conduct regular telephone conferences as deemed necessary or appropriate, to exchange informal information regarding the progress of the Research Program. Each Party may change its designated Project Leader from time to time upon prior written notice to the other Party. Each Project Leader may designate a substitute to temporarily perform the functions of that Project Leader by prior written notice to the other Party.

  • Development Committee As soon as practicable, the Parties will establish a joint development committee, comprised of at least one (1) and up to two (2) representatives of Omega and at least one (1) and up to two (2) representatives of Acuitas (the “JDC”). One such representative from each Party will be such Party’s Workplan Leader. Each Party may replace its Workplan Leader and other JDC representatives at any time upon written notice to the other Party, provided, however, that each Party shall use reasonable efforts to ensure continuity on the JDC. With the consent of the other Party (which will not be unreasonably withheld, conditioned or delayed), each Party may invite non-voting employees and consultants to attend JDC meetings as necessary, subject to consultant’s agreement to be bound to the same extent as a permitted subcontractor under Section 3.1(i).

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

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