Report descriptions

• Annotated Case Report Forms
  Run this report to generate blank case report forms with specific annotations and information about forms' names, question names, and validations associated with questions in forms.
• Clinical One Training report
  In this report, you view all the in-product training that users have completed for Oracle Clinical One Platform. This report provides evidence that users have completed appropriate system training before they take any actions in the user interface.
• Global Study Roles report
  In this report, you view information about all study roles created for all studies at your organization, including pre-defined study roles created by Oracle and retired study roles.
• Kit Chain of Custody (Blinded) report
  In this report, you receive a blinded view of all kits in a study. When run at the site level, the report describes every transition a kit has made throughout the study, both virtual and physical. The report also includes details on changes made to each kit.
• Kit Chain of Custody (Unblinded) report
  In this report, you get an unblinded view of all the kits in a study. The report shows every transition that a kit has made throughout the study, both physical and virtual, plus the user who made the change, when the change happened, and any comments they provided.
• Kit Dispensation report
  In this report, you view dispensation information for one, several, or all subjects at a site. The report lists the kits that were dispensed to a subject at each event in the study, throughout the life of the study. The report also includes information about replacement kits, so you can see the kits that were dispensed for lost or damaged kits.
• Kit Inventory (Blinded) report
  In this report, you view the current status of all kits in inventory. The kit type descriptions appear for any unblinded kits.
• Kit Inventory (Unblinded) report
  In this report, you view the current status of all kits in inventory, broken down by kit type and by lot. This report shows you the number of kits in each lot and can help you figure out if you need to order another run. This report contains unblinding information, including the description of each kit type.
• Kit Reconciliation report
  In this report, you view all kits with a specific status as part of your kit reconciliation work. This report is designed specifically for clinical research associates (CRAs), though other users might also find it useful.
• Minimization report
  In this report, you are able to view the stratum details for impacted subjects in an existing study.
• Randomization List (Blinded) report
  In this report, you view the current status as well as historical data for every randomization number in the study, as well as the subjects who were assigned each randomization number.
• Randomization List (Unblinded) report
  In this report, you view the current status as well as historical data for every randomization number in the study, as well as the subjects who were assigned each randomization number.
• Rules report
  This report gives you a complete view of all the rules that were created in a study and includes all the changes that were performed for each rule.
• Shipment Order Summary report
  This report provides summary details about the status of each order made in a study.
• Sites and Depots report
  In this report, you view the full list of all the sites, all the depots, or all sites and depots that were added to the study.
• Study Design report
  In this report, you view all the settings specified for your study design, including a list of visits and forms in the study, kit and randomization information, and subject and supply settings.
• Study Enrollment report
  In this report, you view details about enrollment for a study.
• Study Roles report (by study)
  In this report, you view information on all study roles created for a specific study that you're assigned to. The report includes information on predefined study roles created by Oracle, as well as data on retired study roles.
• Subject Data for CTMS report
  In this report, you view all subject data at multiple sites within your study. This report is designed specifically for studies that need to send subject information to their clinical trial management system. Only a study team member with the required user roles can run and download this report.
• Subject Data report
  In this report, you view all data collected on every form in the study, including the study version that the data was collected on.
• Subject Dispensation report
  In this report, you view dispensation information for a subject at a site.
• Subject Events report
  In this report, you view all actions that have occurred to each subject, all in a single location.
• Subject Queries report
  In this report, you view query information.
• Subject Visits (Blinded) report
  In this report you view blinded details about each subject's visits and their treatments. With this report you get a complete view of each subject's visit scheduled, including completed visits and projected appointments.
• Subject Visits (Unblinded) report
  This report offers details about the subject's visits and treatment, such as kit ID, kit description, and the anticipated number of kits to be dispensed in future visits.
• Titration Summary report
  In this report, you view at a glance all visits for each subject, along with the titration details for each visit. This report is useful for blinded users who need to verify dispensation and titration data at a site for one or multiple subjects.
• Titration Summary (Unblinded) report
  In this report, you view titration details for all subjects and visits at a site or at multiple sites. This report is useful for unblinded users who want to verify dispensation and titration data at a site, as well as treatment arm information.
• User Assignment reports
  User Assignment reports can help you identify and resolve issues related to user management, as well as give you valuable data on study access at your organization.
• User Upload Error report
  This report contains errors encountered when importing the User Upload Template.