Siebel Clinical Trial Management System 24.4

Siebel Clinical Trial Management System (CTMS) enables global clinical organizations to manage critical clinical trial activities and improve relationships with investigators, from early to late-stage clinical trials.

Siebel Clinical Trials Management System (CTMS) provides Site Visit and Trip Reports functionality to conduct clinical site monitoring as required by industry guidance and regulations. These are some of the most widely used features in Siebel CTMS on the desktop or mobile. These new features provide more consistency between CTMS Mobile Site Visits on tablets and the desktop version of Site Visits. The new functionality includes mobile capabilities, such as support for adding attendees, comments, and subject accrual snapshots, as well as SmartScript functionality in trip report questions and improved navigation for mobile trip reports.

Mobile offline capabilities are now available that can help to manage limited or unreliable internet/Wi-Fi connectivity in hospitals, medical centers, clinics, doctor’s offices, and remote areas where clinical trials may be conducted. With these capabilities, Clinical Research Associates can complete trip reports in a mobile offline mode if there’s unreliable connectivity at the site or work on the trip report while traveling.

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.

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