Data Packages Sample Clauses
The 'Data Packages' clause defines the requirements and standards for the delivery, format, and content of data sets exchanged between parties under the agreement. Typically, this clause specifies what constitutes a complete data package, such as required file types, metadata, documentation, and delivery timelines. For example, it may require that all data be provided in a specific digital format and accompanied by a summary of contents. The core function of this clause is to ensure that data is transferred in a consistent, usable manner, reducing misunderstandings and facilitating efficient data integration or analysis.
Data Packages. With respect to each Research Target, within [***] after the completion of the Development activities set forth in the Research Plan for such Research Target (or, if earlier, [***] prior to the end of the Option Period), Morphic shall deliver to AbbVie the Data Package for such Research Target and shall provide AbbVie with electronic access to all data generated in connection with the Development activities under the Research Plan with respect to such Research Target.
Data Packages. On a Program Slot-by-Program Slot basis, within [***] days after [***] (or such other period of time mutually agreed by the Parties), Caribou shall deliver to AbbVie the complete Data Package with respect to the applicable Program Slot. [***]
Data Packages. On a Target-by-Target basis, C4T shall provide data and results from the activities under the Research Plan to Roche on an ongoing basis during each Stage. Within [***] upon completion of all activities for a Stage, C4T shall prepare and deliver to Roche through the JRC a report summarizing the results and all data from such Stage in the form of a data package for each such Stage as specified in the Research Plan (each, a “Data Package”). Each Data Package shall summarize the results of all activities under the Research Plan for the respective Target, and shall: (a) for Stage 1, identify any Degrader chemical series generated for such Target
Data Packages. (i) As promptly as practicable following completion of each Designated Clinical Trial or other study (including clinical and non-clinical) with respect to a Product conducted by or on behalf of Company during the Company Development Period and, in any event, no later than one hundred twenty (120) days following database lock of such Designated Clinical Trial or other study, Company shall prepare and deliver to Amgen the Data Package for such Designated Clinical Trial or other study. Moreover, during the Company Development Period, Company shall provide to Amgen, when available following database lock of each Designated Clinical Trial, top-line data summaries, summaries of draft data generated prior to completion of the applicable Data Package and raw data from each Designated Clinical Trial. To the extent that Company performs an interim data review, or otherwise reviews or receives material data prior to completion of a Designated Clinical Trial or other study, Company shall promptly make available to Amgen such data and/or the results of such review, as applicable.
(ii) As promptly as practicable following completion of each clinical and non-clinical study with respect to a Product conducted by or on behalf of Amgen during the Company Development Period and, in any event, no later than one hundred twenty (120) days following database lock of such study, Amgen shall prepare and deliver to Company the Data Package for such study. To the extent that Amgen performs an interim data review, or otherwise reviews or receives material data prior to completion of any such study, Amgen shall promptly make available to Company such data and/or the results of such review, as applicable.
Data Packages. With respect to each Data Package, the Party providing such Data Package to the other Party hereby represents and warrants to such other Party, as of the Delivery Date for such Data Package, that to the providing Party’s Knowledge, such Data Package is true, complete and correct.
Data Packages. For each Research Program with respect to a ▇▇▇▇▇▇▇ Antigen, the Research Plan shall describe the contents of the DC Data Package and IND Data Package for such Research Program.
Data Packages. Merus shall: (i) at the direction of the JRC, provide to Incyte the Data Package for Program 1 and Program 2 and their corresponding Bi-Specific Constructs, and (ii) on a Program-by-Program basis, use Commercially Reasonable Efforts to provide to Incyte within [**] (or such other longer period as may be set forth in the applicable Research Plan) following designation of each Target Pair pursuant to Sections 4.4 or 4.5, the Data Package for such Target Pair, including the corresponding General Monoclonal Antibodies, Selected Monoclonal Antibodies and the Bi-Specific Construct(s) that specifically bind to such Target Pair that are the subject of such Program, and which have been the subject of research activities under the applicable Research Plan.
Data Packages. In consideration for providing Data Packages to Hyseq under the Collaboration, Hyseq will pay to Aurora a non-creditable, non-refundable payment of [***] within [***] after delivery of each Data Package to Hyseq. Notwithstanding the foregoing, Hyseq will pay to Aurora a minimum of [***] during the Collaboration Period under this Section 5.1(d).
Data Packages. Merus shall: (i) at the direction of the JRC, provide to Incyte the Data Package for Program 1 and Program 2 and their corresponding Bi-Specific Constructs,
Data Packages. Data packages shall be prepared to support the design review presentations. Generally, the packages for the PDRs, CDRs and FDRs shall be structured to be standalone packages. However, for all CDRs, Category C unit FDRs, and the system FDR, detailed materials (e.g., analyses provided as appendices) provided at the respective PDR, which have not changed, need not be resubmitted. For Category A and B unit FDRs and for all subsystem FDRs, the data packages shall be comprehensive standalone packages. Each shall include all design details, analysis data, qualification test results, design verification test results, and all updated data from PDRs and CDRs. All data packages shall comply with the requirements given in the CDRL description (Appendix 2).