Siebel Clinical Trial Management System 20.7
Siebel Clinical Trial Management System enables global clinical organizations to manage critical clinical trial activities and improve relationships with investigators, from early to late-stage clinical trials.
Clinical Features Updates
Blinded and Unblinded User Access for Clinical Trials
- Siebel Clinical Trial Management System now supports blinded and unblinded user access permissions; for example, unblinded data in Site Visits, Activities, and Document Tracking is hidden for designated blinded users.
- A new Site Visit view is now available under the Administration-Clinical view for administrators to have a consolidated view of all blinded and unblinded site visit data.
Siebel Clinical Task-Based UI
- Task-Based UI is a set of pre-defined interactive procedures with built-in validations that allow the user to perform tasks in a step-wise workflow, offering customers a standard process for study builds and site entries across their global organization and maximizing user efficiency and data quality.
- Supports forward and backward screen navigation.
- Provides additional capabilities to pause a task and resume at a later time, or assign a task to a different user.
- Includes out-of-the-box tasks for users to leverage, such as creating a protocol, region, site, site contacts, activity plans, and a risk assessment (RACT).
Additional information
For further details, refer to the Siebel Clinical Trial Management System Guide.
As always, we are committed to your success with the software and we thank you for your continued support.
Need assistance?
For Technical Support, visit Oracle Health Sciences Support.
As always, we are committed to your success with the software and we thank you for your continued support.
Need assistance?
For Technical Support, visit Oracle Health Sciences Support.