Common use of Study Data Clause in Contracts

Study Data. For each Study, the Institution and the applicable Principal Investigator acknowledge and agree that the data collected during the Study (“Study Data”), except as otherwise provided in Section 15.8, is owned by SPONSOR. SPONSOR may use all Study Data collected during the Study for any and all purposes at the sole discretion of SPONSOR, provided it is consistent with Applicable Laws and regulations, this Agreement and the informed consent form signed by the Subject. Study Data is confidential, and Institution agrees that premature disclosures of the data may be misleading. If the Study is a Multi-Center Study, then after the completion, or earlier termination, of the Study at all participating sites, SPONSOR shall conduct, or cause to be conducted, such analyses of the data resulting from each site participating in the Multi-Center Study (“Multi-Center Study Analyses”) and, if requested, deliver the results of such analyses (“Multi-Center Study Results”) to the applicable Principal Investigator together with the underlying data relating only to Subjects enrolled in the Study at the Institution (“Site Data”), but not any other data and databases that are supplied, prepared, collected, developed or generated as a result of, in the performance of, or in connection with the Multi-Center Study at non Institution sites (“Multi-Center Study Data”). Further, for a Multi-Center Study, the SPONSOR, or its designee, shall have the right to coordinate one or more publications of the Multi-Center Study Results (each, a “Publication”). In case the Study is being conducted solely at the Institution, the SPONSOR will make the data available to the applicable Principal Investigator at the completion or earlier termination of the Study. Any access by Institution and/or its Principal Investigator to the Study Data from all Study sites for Institution and/or Principal Investigator will be addressed in the Study SOW.

Study Data. For each Study, the Institution and the applicable Principal Investigator acknowledge and agree that the data collected during the Study as required by the applicable Protocol (“Study Data”), except as otherwise provided in Section 15.8, is owned by SPONSOR. SPONSOR may use all Study Data collected during the Study for any and all purposes at the sole discretion of SPONSOR, provided it is consistent with Applicable Laws and regulations, this Agreement and the informed consent form signed by the Subject. Study Data is confidential, and Institution agrees that premature disclosures of the data may be misleading. If the Study is a Multi-Center Study, then after the completion, or earlier termination, of the Study at all participating sites, SPONSOR shall conduct, or cause to be conducted, such analyses of the data resulting from each site participating in the Multi-Center Study (“Multi-Center Study Analyses”) and, if requested, deliver the results of such analyses (“Multi-Center Study Results”) to the applicable Principal Investigator together with the underlying data relating only to Subjects enrolled in the Study at the Institution (“Site Data”), but not any other data and databases that are supplied, prepared, collected, developed or generated as a result of, in the performance of, or in connection with the Multi-Center Study at non Institution sites (“Multi-Multi- Center Study Data”). Further, for a Multi-Center Study, the SPONSOR, or its designee, shall have the right to coordinate one or more publications of the Multi-Center Study Results (each, a “Publication”). In case the Study is being conducted solely at the Institution, the SPONSOR will make the data available to the applicable Principal Investigator at the completion or earlier termination of the Study. Any access by Institution and/or its Principal Investigator to the Study Data from all Study sites for Institution and/or Principal Investigator will be addressed in the Study SOW.

Study Data. For each Study, the Institution and the applicable Principal Investigator acknowledge and agree that the data collected during the Study as required by the applicable Protocol (“Study Data”), except as otherwise provided in Section 15.8, is owned by SPONSOR. SPONSOR may use all Study Data collected during the Study for any and all purposes at the sole discretion of SPONSOR, provided it is consistent with Applicable Laws and regulations, this Agreement and the informed consent form signed by the Subject. Study Data is confidential, and Institution agrees that premature disclosures of the data may be misleading. If the Study is a Multi-Center Study, then after the completion, or earlier termination, of the Study at all participating sites, SPONSOR shall conduct, or cause to be conducted, such analyses of the data resulting from each site participating in the Multi-Center Study (“Multi-Center Study Analyses”) and, if requested, deliver the results of such analyses (“Multi-Center Study Results”) to the applicable Principal Investigator together with the underlying data relating only to Subjects enrolled in the Study at the Institution (“Site Data”), but not any other data and databases that are supplied, prepared, collected, developed or generated as a result of, in the performance of, or in connection with the Multi-Center Study at non Institution sites (“Multi-Center Study Data”). Further, for a Multi-Center Study, the SPONSOR, or its designee, shall have the right to coordinate one or more publications of the Multi-Center Study Results (each, a “Publication”). In case the Study is being conducted solely at the Institution, the SPONSOR will make the data available to the applicable Principal Investigator at the completion or earlier termination of the Study. Any access by Institution and/or its Principal Investigator to the Study Data from all Study sites for Institution and/or Principal Investigator will be addressed in the Study SOW.