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Siebel Life Sciences Guide > Setting Up and Carrying Out a Clinical Trial > End-User Procedures >
Reviewing Documentation for Tracking
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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Siebel Life Sciences Guide Published: 18 April 2003 |