Trial Data. During the course of the Trial, Institution and Principal Investigator will collect and submit certain data to Sponsor or its agent, as specified in the Protocol. This includes CRFs (or their equivalent) or electronic data records, as well as any other documents or materials created for the Trial and required to be submitted to Sponsor or its agent, such as X-ray, MRI, or other types of medical images, ECG, EEG, or other types of tracings or printouts, or data summaries (collectively, “Trial Data”). Institution and Principal Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. a.
Trial Data. Customer agrees that any data or information that Customer enters into the Services used on a Trial Basis, and any customizations made to such Services by or for Customer, during the Trial Basis period may be permanently lost unless Customer purchases the same Services on a non-Trial Basis before the termination date set forth in Section 4.2 above.
Trial Data. During the course of the Trial, Institution and Principal Investigator will collect and submit certain data to Sponsor or its agent, as specified in the Protocol. This includes CRFs (or their equivalent) or electronic data records, as well as any other documents or materials created for the Trial and required to be submitted to Sponsor or its agent, such as X-ray, MRI, or other types of medical images, ECG, EEG, or other types of tracings or printouts, or data summaries (collectively, “Trial Data”). Institution and Principal Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. 12.1. Údaje klinického hodnocení V průběhu klinického hodnocení mohou zdravotnické zařízení a hlavní zkoušející shromažďovat a předávat určitá data zadavateli nebo jeho zástupci, jak je uvedeno v protokolu. Patří sem formuláře CRF (nebo jejich ekvivalent) nebo elektronické záznamy údajů a dále všechny další dokumenty a materiály vytvořené pro klinické hodnocení, které musí být předloženy zadavateli nebo jeho zástupci, např. rentgenové snímky, snímky MR nebo jiné typy zdravotních snímků, EKG, EEG nebo jiné typy záznamů nebo výtisků vyšetření nebo souhrny údajů (společně jako “údaje klinického hodnocení”). Zdravotnické zařízení a hlavní zkoušející zajistí přesné a včasné shromažďování, zaznamenání a předkládání údajů klinického hodnocení.
Trial Data. During the course of the Trial, Institution and Principal Investigator will collect and submit certain data to Sponsor or its agent, as specified in the Protocol. This includes CRFs (or their equivalent) or electronic data records, as well as any other documents or materials created for the Trial and required to be submitted to Sponsor or its agent, such as X-ray, magnetic resonance imaging (“MRI”), or other types of medical images, electrocardiogram (“ECG”), electroencephalography (“EEG”), or other types of tracings or printouts, or data summaries (collectively, “Trial Data”). Principal Investigator shall ensure that Research staff will accurate and timely collect, record, and submit Trial Data. 12.1.
Trial Data. Any data or information that Subscriber enters into the Services used on a Trial Basis, and any customizations made to such Services by or for Subscriber, during the Trial Basis period may be permanently lost unless Subscriber purchases the same Services on a non-Trial Basis before the termination date set forth in Section 5.2 above.
Trial Data. During the course of the Trial, Institution and Investigator will collect and submit to Sponsor or its designee all data generated in the conduct of the Trial including, without limitation, completed case report forms in the form and/or electronic medium supplied or specified by Sponsor or its designee (“CRFs”), X-rays, MRIs or other types of medical images, ECGs, EEGs or other types of tracings or printouts, and data summaries (collectively, the “Trial Data”). Institution and Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. Sponsor is the exclusive owner of all Trial Data. 8.1 Data ze studie. V průběhu studie budou zdravotnické zařízení a zkoušející shromažďovat a předkládat zadavateli nebo jeho pověřené osobě veškerá data vytvořená při provádění studie, mimo jiné včetně vyplněných záznamů subjektů hodnocení na formuláři a/nebo elektronickém médiu, které dodá nebo stanoví zadavatel nebo jeho pověřená osoba (dále jako „CRF“), RTG snímků, snímků z MR nebo jiných vyšetření, záznamů EKG, EEG nebo jiných druhů sledování nebo počítačových výpisů a shrnutí dat (souhrnně jako „data ze studie“). Zdravotnické zařízení a zkoušející zajistí přesné a včasné shromažďování, zaznamenání a odeslání dat ze studie. Zadavatel je výhradním majitelem veškerých dat ze studie.
Trial Data. During the course of the Trial, Principal Investigator will collect and submit certain data to Sponsor or its agent, as specified in the Protocol. This includes CRFs (or their equivalent) or electronic data records, as well as any other documents or materials created for the Trial and required to be submitted to Sponsor or its agent, such as X-ray, MRI, or other types of medical images, ECG, EEG, or other types of tracings or printouts, or data summaries (collectively, “Trial Data”). Principal Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. 11.1
Trial Data. Data o klinickém výzkumu. During the course of the Trial, Health Service Provider and PI shall collect and submit certain data to Sponsor or its third party vendors, including CRO, as specified in the Protocol, including Trial Data. Trial Data shall generally be submitted within ten working days from its collection. All queries must be resolved within five (5) days of receipt of such queries by Health Service Provider and/or PI at any time during the Trial. These periods could be shorter if this is required by special circumstances (such as patient safety is at risk, database closure, interim analysis etc.). Health Service Provider shall ensure accurate and timely collection, recording, and submission of Trial Data.
Trial Data. For each Trial, the Institution and the applicable Principal Investigator acknowledge and agree that the data collected during the Trial as required by the applicable Protocol (“Trial Data”), except as otherwise provided in Section 15.8, is owned by SPONSOR. SPONSOR may use all Trial Data collected during the Trial 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. Trial Data is confidential, and Institution agrees that premature disclosures of the data may be misleading. If the Trial is a Multi-Center Trial, then after the completion, or earlier termination, of the Trial 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 Trial (“Multi-Center Trial Analyses”) and, if requested, deliver the results of such analyses (“Multi-Center Trial Results”) to the applicable Principal Investigator together with the underlying data relating only to Subjects enrolled in the Trial 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 Trial at non Institution sites (“Multi-Center Trial Data”). Further, for a Multi-Center Trial, the SPONSOR, or its designee, shall have the right to coordinate one or more publications of the Multi-Center Trial Results (each, a “Publication”). In case the Trial 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 Trial. Any access by Institution and/or its Principal Investigator to the Trial Data from all Trial sites for Institution and/or Principal Investigator will be addressed in the Trial SOW.
Trial Data. During the course of the Trial, Institution and Investigator will collect and submit to Sponsor or its designee all data generated in the conduct of the Trial (the “Trial Data”). Trial Data, includes, without limitation, completed case report forms in the form and/or electronic medium supplied or specified by Sponsor or its designee (“CRFs”), X- rays, MRIs or other types of medical images, ECGs, EEGs or other types of tracings or printouts, and data summaries, as well as any other documents or materials resulting from the conduct of the Trial. Institution and Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. Sponsor is the exclusive owner of all Trial Data. 9.1
