Research Activities. Uncertainties of effects and results are typical to all re- search and development activities and specific outcomes of the activities in the Project cannot be guaranteed. The Parties acknowledge and accept these uncertainties and agree not to bring any claims against any other Party to this Agreement, pertaining to the anticipated outcome or the results and success of the Project.
Research Activities. Research results obtained (including a short description of progress on the individual projects) and deviations, if any, to the original research work plan. • Scientific highlights and achievements (scientific/technological breakthrough, patents, awards, prizes etc...). • A full list of individual and joint publications, directly related to the work undertaken within the project (including citation index and impact factor), with appropriate acknowledgment of the funding source. • Intersectoral and multidisciplinary collaboration.
Research Activities. 5.1 Following the designation of a Collaboration Target as an Approved Collaboration Target, the Parties shall commence the Small Molecule Research Project for that Approved Collaboration Target in accordance with this Agreement (including the Research Plan for that Approved Collaboration Target), provided that: (a) there will be no more than [***] active Small Molecule Research Projects (for clarity, excluding any Research Program for a Collaboration NSM Target) at any given time during the Research Term; and (b) the maximum number of active Small Molecule Research Projects in sub-clause (a) will [***] each time [***] Collaboration Development Candidates are selected for an Approved Collaboration Target in accordance with Clause 6.1. For the avoidance of doubt, if one or more Collaboration Development Candidates are selected for [***] Approved Collaboration Targets, neither Party shall be required to carry out any further Small Molecule Research Projects.
5.2 Each Party shall use Commercially Reasonable Efforts to undertake those activities allocated to it in each Research Plan and NSM Research Plan in accordance with such Research Plan or NSM Research Plan and this Agreement. Each Party shall comply with Applicable Laws in performing those activities allocated to it in the Research Plan.
5.3 Each Party shall ensure that all of its personnel engaged in the performance of any of that Party’s responsibilities under each Research Plan or NSM Research Plan (a) are competent and efficient; and (b) have appropriate and relevant qualifications, training and experience for, and are knowledgeable about, that Party’s responsibilities under that Research Plan or NSM Research Plan.
5.4 Any Research Plan or NSM Research Plan may be amended from time to time by the Joint Steering Committee in accordance with Clause 11.
5.5 Each Party (the “Subcontracting Party”) may engage an Affiliate or Third Party subcontractor to perform any of its responsibilities under a Research Plan; provided that:
(a) prior to [***] subcontracting such performance to Third Party subcontractors, [***] shall obtain the prior written consent of [***] it being agreed that the subcontractors listed on Schedule 2 are pre-agreed as of the Effective Date);
(b) that Affiliate or subcontractor meets the qualifications and standards generally required by the Subcontracting Party for the performance of work similar in scope and complexity to the subcontracted activity;
(c) the Subcontracting Party ensures...
Research Activities. Following the JRC’s approval of a Research Plan, each Party will use Commercially Reasonable Efforts to perform activities for which such Party is responsible under such Research Plan in accordance with the timelines set forth therein. Vertex will be responsible for carrying out all Vertex Activities under a Research Plan, and CRISPR will be responsible for carrying out all CRISPR Activities under each Research Plan. Each Party will, and will require its Affiliates and Subcontractors to, comply with all Applicable Laws in its and their conduct of the activities under a Research Plan, including where appropriate cGMP, GCP and GLP (or similar standards). No more than [***] Research Plans shall be conducted at any given time during the Initial Target Selection Period and no more than [***] Research Plans shall be conducted at any given time during the Final Target Selection Period. CRISPR will dedicate such number of FTEs as is reasonably required to perform the CRISPR Activities under the Research Plans during the Target Selection Period, which CRISPR currently anticipates will be no fewer than an average of [***] FTEs to the performance of Research Plans during the Initial Target Selection Period and no fewer than an average of [***] FTEs to the performance of Research Plans during the Final Target Selection Period.
Research Activities. 14 2.1 RiboGene Efforts ........................................14 2.2
Research Activities. 2.1 RiboGene Efforts RiboGene shall use all reasonable efforts to expeditiously perform its part of the Research Program substantially in accordance with the terms and conditions of this Agreement, including the descriptions and timetables of the Annual Research Plans and any additional specifications as may be proposed by the JMT and agreed upon in writing by the parties hereto from time to time during the Research Term.
2.2 Abbott Efforts Abbott shall expend at least [*] per year in support of its own activities under the Research Program, in addition to its separate, but related support of RiboGene's activities, according to the provisions of Section 4.1; shall identify, at its sole option, and permit RiboGene to use pertinent Abbott technology, only during the Research Term, and only for purposes of the Program; and will provide to RiboGene such of its research data, results and conclusions which it deems necessary to accomplish the objectives of the Research Program.
Research Activities. During the Research Term for each Research Program, Morphic will keep Xxxxxxx reasonably informed, through the JRC, regarding the status and progress of Morphic’s activities under such Research Program, including the status of all Morphic Research Activities. During the Research Term for a Research Program, on a Calendar Quarterly basis, Morphic will prepare and provide to the JRC written reports on the status of all such Morphic Research Activities performed under such Research Program during the applicable Calendar Quarter. Such quarterly reports will include, with respect to such Research Program, the characteristics of any Compounds identified, the selection of Compounds for further study (including those for which Xxxxxxx may determine to commence Late Lead Optimization Activities following the completion of Lead Optimization Activities for such Research Program in accordance with Section 2.5 (Late Lead Optimization Activities)), completed Morphic Research Activities required for Xxxxxxx to commence IND-Enabling Studies for such Research Program and the Prosecution and Maintenance of any Morphic Patents or Joint Patents Covering any such Compounds. Such reports must be sufficient in content to allow Xxxxxxx to evaluate the progress of the Morphic Research Activities against the objectives and timelines included therefor in the applicable Research Plan. In addition, Morphic will promptly report any other Results of a Research Program that are reasonably likely to be significant to the JRC. At any time during the Option Period for a Research Program, Morphic will promptly respond to any reasonable inquiries from Xxxxxxx regarding the progress of activities under such Research Program (including any Morphic Research Activities).
Research Activities. During the term of this Agreement, the parties will conduct such collaborative research and development of Products as they may mutually agree upon in writing in the Research Plan (as the same may be amended from time to time). During the term of this Agreement, GNE and ABX shall each update the other, as requested by the other, as to the status of any research activities of the party under the Research Plan.
Research Activities. General progress with research activities programmed at individual, participant team and network level. Possible problems encountered and nature/justification for adjustments, if any, to the original research work plan and/or timetable.
Research Activities. Morphic will transfer to Xxxxxxx copies of any and all Morphic Know-How that is necessary or useful for the performance of all Xxxxxxx Research Activities (a) no later than [***] after the Effective Date and (b) no later than [***] after the selection of any Replacement Target MoA by Xxxxxxx in accordance with Section 2.6.1 (Replacement Decisions). Each Calendar Quarter during the remainder of the Research Term for a Research Program, Morphic will transfer to Xxxxxxx copies of any Morphic Know-How that is related to the Xxxxxxx Research Activities under such Research Program and that is made, conceived, discovered or otherwise generated since the previous transfer of such Know-How to continue to enable Xxxxxxx to perform such Xxxxxxx Research Activities. Notwithstanding anything to the contrary set forth in this Agreement, Morphic will not, and will cause its Affiliates not to, disclose to Xxxxxxx or any of its Affiliates any Know-How licensed to Morphic under the CMCC License Agreement.
