Research Program Activities definition

Research Program Activities has the meaning specified in Section 2.1.1 hereof.
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Research Program Activities means discrete activities, and/or phases of research that are carried out under the Consortium’s Research Program.
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Research Program Activities means all Development activities performed by or on behalf of a Party pursuant to this Project Agreement. For clarity, Research Program Activities can be with respect to Clinical Development (i.e., Clinical Development Research Program Activities) or Preclinical Research (i.e., Preclinical Research Program Activities).
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Examples of Research Program Activities in a sentence

  • The Clinical Research Plan will include: (a) a description of the Research Program Activities and each Party’s obligations in connection therewith; (b) the projected timelines for completion of the Research Program Activities; (c) an estimated budget for the Clinical Development activities (the “Clinical Development Budget”); and (d) a clinical trial synopsis with respect to the Clinical Study.

  • In the event that this Project Agreement is terminated for any reason prior to Clinical Study Completion, Immatics shall responsibly wind-down the Research Program Activities, and Moderna will reasonably assist Immatics (including provision of supply) with respect to such wind-down, in accordance with accepted biopharmaceutical industry norms and ethical practices and Moderna shall reimburse Immatics for all reasonably documented costs associated with such wind-down activities.

  • Without limiting Section 4.4.1, each Party shall deliver to the other Party, at least five Business Days prior to each regular Clinical Study Project Committee meeting, a reasonably-detailed written report regarding such Party’s Research Program Activities (if any) and all progress and Research Program Results since the Clinical Study Project Committee’s prior meeting (or, with respect to the first Clinical Study Project Committee meeting, since the Effective Date) (each, a “Research Program Report”).

  • Immatics shall initially set up, hold, and maintain the global safety database for the Clinical Study with respect to safety data obtained in connection with the Research Program Activities.

  • Subject to Section 8.2.2, Moderna shall be responsible for all Clinical Development Research Program Costs incurred by either Party in connection with Clinical Development Research Program Activities under the Clinical Research Plan.

  • Each Party shall: (a) conduct all Research Program Activities allocated to it in accordance with the Clinical Research Plan, in good scientific manner, in compliance with all Applicable Laws, and, subject to Article 8, at its sole cost and expense; and (b) [***] perform such obligations within the applicable timelines set forth in the Clinical Research Plan.