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Siebel Life Sciences Guide > Setting Up and Carrying Out a Clinical Trial > End-User Procedures >

Reviewing Documentation for Tracking

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The CRAs review all the documentation required for meeting regulatory requirements at the site and assure that review deadlines are met.

To review and track documentation

Navigate to the Site Management screen.
From the Show drop-down list, select My Sites.
In the Sites list, query for the site for which you want to review documentation.
Click the Document Tracking view.

The Document Tracking list shows the required documents.

Optional: Complete the necessary fields to maintain a record of document events.

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