Common use of Trial Data Clause in Contracts

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. During the course of the Trial, Institution Provider 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”). Provider and Principal Investigator shall will ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.1.a.

Trial Data. During the course of the Trial, Institution Provider 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”). Provider and Principal Investigator shall will ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.1.

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”). Institution and Principal Investigator shall will ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.1.12.0

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”). Institution and Principal Investigator shall will ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.1a záznamy.

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 of Trial Data. 12.1.

Trial Data. During the course of the Trial, Institution and and/or 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”). Institution and/or Principal Investigator Investigatory shall ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.110.1.

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 will ensure that Research staff will accurate and timely collectcollection, recordrecording, and submit submission of Trial Data. 12.1.